EP2070988A2 - Styryl thiol/disulfide compound with a hydroxy(cyclo)alkylamino unit, process for lightening keratin materials using this dye - Google Patents

Abstract

Styryl hydroxy(cyclo)alkylamino thiol/disulfide compounds (I) and their organic or inorganic acid salts, optical isomers, geometrical isomers or solvates such as hydrates, useful as fluorescent dye, are new. Styryl hydroxy(cyclo)alkylamino thiol/disulfide compounds of formula (I) and their organic or inorganic acid salts, optical isomers, geometrical isomers or solvates such as hydrates, useful as fluorescent dye, are new. Either R 1 : 1-6C alkyl substituted by one or more OH groups; and R 2 : 1-6C alkyl optionally substituted by one or more OH groups; or NR 1R 2 : saturated heterocyclic radical substituted by OH, (poly)hydroxy(1-4C)alkyl or -C(O)OR1a; R1a : H, 1-4C alkyl or -C(O)-O ->(in which anionic counter ion (An ->) is absent); R 3 : N or -C(O)OR1b; R1b : H, alkaline metal, 1-6C alkyl or -C(O)-O ->(in which anionic counter ion (An ->) is absent); Z : -C(O)-N(R)-, -N(R)-C(O)- or 1-10C divalent alkylene interrupted by amido group -C(O)-N(R)- or -N(R)-C(O)-; n : 1 or 2; m : 0 or 1; An -> : anionic counter ion; Y 1 : H, alkaline metal (both preferred), alkaline-earth metal, ammonium group (N +>Ralpha Rbeta Rgamma Rdelta ), phosphonium group (p +>Ralpha Rbeta Rgamma Rdelta ) or thiol protecting group; and Ralpha , Rbeta , Rgamma , Rdelta : H or 1-4C alkyl. Provided that when: n and m are 1, then Y 1is H or protecting group of thiol function; and n is 2, then m is 0; and (I) contains other cations, it is associated to one or more counter anionic ion to achieve the electroneutrality of (I). Where the bond between the pyridinium cycle and the double bond of the styryl group is positioned in 2 or 4 position of pyridinium. Independent claims are included for: (1) a coloring composition comprising (I), in a medium; (2) a method for coloring keratin materials comprising applying the composition on the keratin materials optionally in the presence of reducing agent; and (3) a device with several compartments comprising a first compartment comprising a coloring composition comprising (I) and a second compartment comprising a reducing agent. [Image].

Description

The invention relates to the dyeing of keratin materials using styryl hydroxy (cyclo) alkylamino thiol / disulfide fluorescent dyes.

It is known to dye keratinous fibers, especially human fibers, by direct dyeing. The method conventionally used in direct dyeing consists in applying to the keratin fibers direct dyes which are colored and dyeing molecules having an affinity for the fibers, allowing them to diffuse and then rinsing the fibers.

The direct dyes which are conventionally used are, for example, dyes of the nitrobenzene type, anthraquinone dyes, nitropyridines, dyes of the azo, xanthene, acridine, azine or triarylmethane type.

The coloring of the keratinous fibers from these conventional direct dyes does not make it possible to significantly lighten the keratin fibers.

The lightening of the color of dark keratin fibers to lighter shades, possibly modifying the shade of these, constitutes an important demand.

Conventionally, to obtain a lighter color, a chemical bleaching process is used. This method consists in treating the keratinous fibers, such as the hair, with a strong oxidizing system, generally consisting of hydrogen peroxide associated or not with persalts, most often in an alkaline medium.

This bleaching system has the disadvantage of degrading the keratinous fibers, and altering their cosmetic properties. The fibers tend to become rough, more difficult to disentangle and more fragile. Finally, the lightening or the bleaching of keratinous fibers by oxidizing agents is incompatible with the treatments for modifying the shape of said fibers, particularly in the straightening treatments.

Another lightening technique consists in applying fluorescent direct dyes to dark hair. This technique described in particular in the documents WO 03/028685 , WO 2004/091473 allows to respect the quality of the keratinous fiber during the treatment. However, these fluorescent direct dyes do not have a satisfactory tenacity vis-à-vis the external agents.

To increase the tenacity of the direct dyes, it is known to use disulfide dyes, in particular dyes with chromophore aza-imidazoliums, in patent applications. WO 2005/097051 or EP 1647580 , and pyridinium / indolinium-styryl chromophore dyes in patent applications WO 2006/134043 and WO 2006/136617 .

The object of the present invention is to provide novel systems for dyeing keratin materials, in particular human keratinous fibers, in particular the hair, which do not have the drawbacks of existing bleaching processes.

In particular, it is an object of the invention to provide direct dyeing systems which make it possible to obtain lightening effects, in particular on naturally or artificially dark keratin fibers, which are stubborn in the face of successive shampoos, which do not degrade keratin fibers and which do not degrade. do not alter their cosmetic properties.

Another object of the invention is to color chromatically and remanent vis-à-vis the external aggressions keratin materials. The invention also aims to provide compounds dyeing keratinous fibers such as hair with a low selectivity of coloration between the root and the tip, whether on natural or permed fibers.

leurs sels d'acide organique ou minéral, isomères optiques, isomères géométriques, et les solvates tels que hydrates ; formule (I) dans laquelle :

• R₁ , représente un groupe alkyle en C₁-C₆ substitué par un ou plusieurs groupes hydroxyle ou -C(O)OR' avec R' représentant un atome d'hydrogène, un groupe alkyle en C₁-C₄ ou alors un groupe -C(O)-O^- et dans ce dernier cas un contre ion anionique An^- est absent, particulièrement R₁ représente un groupe alkyle en C₁-C₆ substitué par ou plusieurs groupes hydroxyle et plus spécifiquement par un seul groupe hydroxyle ;
• R₂ , représente un groupe alkyle en C₁-C₆ éventuellement substitué par un ou plusieurs groupes hydroxyle ;
• ou alors les groupements R₁ et R₂ forment ensemble avec l'atome d'azote qui les portent un radical hétérocyclique saturé substitué au moins par un groupement hydroxyle, (poly)hydroxy(C₁-C₄)alkyle, et/ou -C(O)OR' avec R' représentant un atome d'hydrogène, un groupe alkyle en C₁-C₄ ou alors un groupe -C(O)-O- et dans ce cas un contre ion anionique An^- est absent, ; tel que pyrrolidinyle et pipéridyle ;
• R₃ représente un atome d'hydrogène ou un groupement -C(O)OR" avec R" représentant un atome d'hydrogène, un métal alcalin, un groupement alkyle en C₁-C₆ ou alors R₃ représente un groupe -C(O)-O- et dans ce cas un contre-ion anionique An^- est absent ;
• Z représente un groupe divalent amido -C(O)-N(R)-, -N(R)-C(O)-, ou un groupe divalent alkylène en C₁-C₁₀ interrompu par un groupe amido -C(O)-N(R)-, -N(R)-C(O)-tel que -(CH₂)_n'-C(O)-N(R)-(CH₂)_p-, -(CH₂)_n"-N(R)-C(O)-(CH₂)_p-, avec n' représentant un entier compris inclusivement entre 0 et 3, préférentiellement n' vaut 0, 2, 3 ; p représentant un entier compris inclusivement entre 0 et 4, n" représentant un entier compris inclusivement entre 0 et 3 et notamment n'=n"=p=0 et R représentant un atome d'hydrogène ou un groupe alkyle en C₁-C₆ ;
• n vaut 1 ou 2 ;
• m vaut 0 ou 1 ;
• An^- représente un contre ion anionique ;
• Y représente : i) un atome d'hydrogène, ii) un métal alcalin, iii) un métal alcalino-terreux, iv) un groupe ammonium : N⁺R^αR^βR^γR^δ, un groupe phosphonium : P⁺R^αR^βR^γR^δ avec R^α, R^β, R^γ et R^δ, identiques ou différents, représentant un atome d'hydrogène ou un groupe (C₁-C₄)alkyle, ou v) un groupe protecteur de fonction thiol ; étant entendu que :
  • la liaison entre le cycle pyridinium et la double liaison du groupe styryle est positionnée en position 2 ou 4 du pyridinium ;
  • lorsque n=1, m=1 alors Y = H ou groupe protecteur de la fonction thiol et lorsque n=2, alors m=0
  • lorsque le composé de formule (I) contient d'autres parties cationiques, il se trouve associé à un ou plusieurs contre-ions anioniques permettant d'atteindre l'électroneutralité de la formule (I).

These objects are achieved with the present invention which relates to a process for dyeing keratin materials, in particular keratin fibers, in particular human fibers such as the hair, more particularly the dark hair, consisting in applying to the keratin materials a dye composition. comprising, in a suitable cosmetic medium, at least one disulfide or thiol fluorescent dye chosen from the dyes of formula (I) :

their organic or inorganic acid salts, optical isomers, geometric isomers, and solvates such as hydrates; formula (I) in which:

• R ₁ represents a C ₁ -C ₆ alkyl group substituted by one or more hydroxyl groups or -C (O) OR 'with R' representing a hydrogen atom, a C ₁ -C ₄ alkyl group or a -C (O) -O group ^- and in the latter case anionic counterion An ^- is absent, particularly R ₁ represents a C ₁ -C ₆ alkyl group substituted by one or more hydroxyl groups and more specifically by a single hydroxyl group ;
• R ₂ represents a C ₁ -C ₆ alkyl group optionally substituted with one or more hydroxyl groups;
• or else the groups R ₁ and R ₂ together with the nitrogen atom carrying them form a saturated heterocyclic radical substituted at least by a group hydroxyl, (poly) hydroxy (C ₁ -C ₄ ) alkyl, and / or -C (O) OR 'with R' representing a hydrogen atom, a C ₁ -C ₄ alkyl group or a -C group (O) -O- and in this case an anionic counterion An ^- is absent,; such as pyrrolidinyl and piperidyl;
• R ₃ represents a hydrogen atom or a -C (O) OR "group with R" representing a hydrogen atom, an alkali metal, a C ₁ -C ₆ alkyl group or R ₃ represents a -C group (O) -O- and in this case an anionic counterion An ^- is absent;
• Z represents a divalent amido group -C (O) -N (R) -, -N (R) -C (O) -, or a divalent group C ₁ -C ₁₀ alkylene interrupted by an amido group -C (O ) -N (R) -, -N (R) -C (O) -that - (CH ₂ ) _{n '} -C (O) -N (R) - (CH ₂ ) _p -, - (CH ₂ ) _{n "} -N (R) -C (O) - (CH ₂ ) _p -, where n 'is an integer between 0 and 3, preferably n' is 0, 2, 3, p is an integer inclusive between 0 and 4, n "representing an integer inclusive between 0 and 3 and in particular n '= n" = p = 0 and R representing a hydrogen atom or a C ₁ -C ₆ alkyl group;
• n is 1 or 2;
• m is 0 or 1;
• An ^- represents anionic counterion;
• Y represents: i) a hydrogen atom, ii) an alkali metal, iii) an alkaline earth metal, iv) an ammonium group: N ⁺ R ^α R ^β R ^γ R ^δ , a phosphonium group: P ⁺ R ^α R ^β R ^γ R ^δ with R ^α , R ^β , R ^γ and R ^δ , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ ) alkyl group, or v) a protecting group of thiol function ; Being heard that :
  • the bond between the pyridinium ring and the double bond of the styryl group is positioned in position 2 or 4 of the pyridinium;
  • when n = 1, m = 1 then Y = H or protecting group of the thiol function and when n = 2, then m = 0
  • when the compound of formula (I) contains other cationic parts, it is associated with one or more anionic counter-ions making it possible to reach the electroneutrality of formula (I) .

Another subject of the invention is a dyeing composition comprising, in a suitable cosmetic medium, at least one thiol / disulfide fluorescent dye (I) as defined above, and optionally a reducing agent.

The invention also relates to new thiol / disulfide fluorescent dyes of formula (I) .

The dyeing process according to the invention makes it possible to visibly stain dark keratin materials, in particular dark human keratin fibers, especially the dark hair.

In addition, the process of the invention makes it possible to obtain a coloration of the keratin materials, in particular human keratinous fibers, in particular the hair, without degrading said material, which is persistent with respect to shampoos, of the common aggressions (sun, perspiration). , and other hair treatments. The process of the invention also makes it possible to obtain a lightening of keratin materials such as keratinous fibers, particularly dark keratinous fibers and more particularly dark hair.

The new dyes according to the invention have a very satisfactory photostability and chemical stability. These dyes are soluble in cosmetic media suitable for hair dyes and especially in water / ethanol mixtures. They make it possible to extend the accessible color range (yellow, orange, red dyes) while leaving the possibility of stripping the obtained colorings.

The dyes of formula (I) color after application on keratin fibers chromatically and remanent vis-à-vis the external aggressions keratin materials with a low selectivity of coloration between the root and the tip, and on different types of fibers.

For the purposes of the invention, dark keratin material is understood to mean that which has an L * luminescence in the C.I.E. L * a * b *, less than or equal to 45 and preferably less than or equal to 40, knowing moreover that L * = 0 is equivalent to black and L * = 100 to white.

For the purposes of the invention, the term naturally or artificially dark hair, hair whose pitch is less than or equal to 6 (dark blonde) and preferably less than or equal to 4 (chestnut).

The lightening of the hair is evaluated by the variation of "pitch" before and after application of the compound of formula (I) . The notion "tone" is based on the classification of natural nuances, a tone separating each nuance from that which follows or immediately precedes it. This definition and the classification of natural shades is well known to hair professionals and published in the book "Science of hair treatments" by Charles ZVIAK 1988, Ed Masson, p. 215 and 278 .

Heights range from 1 (black) to 10 (very light blond), a unit corresponding to a tone; the higher the number, the clearer the nuance.

An artificially colored hair is a hair whose color has been modified by a coloring treatment, for example a coloration with direct dyes or oxidation dyes.

For the purposes of the invention, the term "bleached hair" means hair whose pitch is greater than 6 and preferably greater than 7.

For the purposes of the invention, the term "stripping" of the coloration of keratin fibers is a process that involves the application of a chemical or physical stimulus capable of bringing the hair back to its original color. By way of example, the etching may be obtained by applying an oxidizing composition based on hydrogen peroxide, sodium persulfate, potassium or ammonium, at a moderately alkaline pH, ie between 7 and 12, preferably between 8 and 10.5.

One means for measuring the lightening effect provided to the hair after application of the fluorescent dyes of the invention is to use the hair reflectance phenomenon.

Preferably, the composition should, after application to dark hair bring to the results below.
- We are interested in the reflectance performance of hair when irradiated with visible light in the wavelength range of 400 to 700 nanometers.
The reflectance curves are then compared as a function of the wavelength, of the hair treated with the composition of the invention and of the untreated hair.
- The curve corresponding to the treated hair must show a reflectance in the wavelength range from 500 to 700 nanometers higher than the curve corresponding to untreated hair.
This means that, in the wavelength range of 540 to 700 nanometers, there is at least one range where the reflectance curve corresponding to the treated hair is greater than the reflectance curve corresponding to the untreated hair. The term "superior" means a difference of at least 0.05% reflectance, and preferably at least 0.1%. This does not prevent that there may exist in the wavelength range from 540 to 700 nanometers, at least one range where the reflectance curve corresponding to the treated hair is superimposable, or less than the reflectance curve corresponding to the untreated hair.

Preferably, the wavelength where the difference is greatest between the reflectance curve of the treated hair and that of the untreated hair is in the wavelength range of 500 to 650 nanometers, and preferably in the the wavelength range from 550 to 620 nanometers.

• les radicaux « aryle » ou « hétéroaryle » ou la partie aryle ou hétéroaryle d'un radical peuvent être substitués par au moins un substituant porté par un atome de carbone, choisi parmi :
  • un radical alkyle en C₁-C₁₆, de préférence en C₁-C₈, éventuellement substitué par un ou plusieurs radicaux choisis parmi les radicaux hydroxy, alcoxy en C₁-C₂, (poly)-hydroxyalcoxy en C₂-C₄, acylamino, amino substitué par deux radicaux alkyle, identiques ou différents, en C₁-C₄, éventuellement porteurs d'au moins un groupe hydroxy ou, les deux radicaux pouvant former avec l'atome d'azote auquel ils sont rattachés, un hétérocycle comprenant de 5 à 7 chaînons, de préférence de 5 ou 6 chaînons, saturé ou insaturé éventuellement substitué comprenant éventuellement un autre hétéroatome identique ou différent de l'azote ;
  • un atome d'halogène tel que chlore, fluor ou brome ;
  • un groupe hydroxy ;
  • un radical alcoxy en C₁-C₂ ;
  • un radical alkylthio en C₁-C₂ ;
  • un radical (poly)-hydroxyalcoxy en C₂-C₄ ;
  • un radical amino ;
  • un radical héterocycloalkyle à 5 ou 6 chaînons ;
  • un radical hétéroaryle à 5 ou 6 chaînons éventuellement cationique, préférentiellement imidazolium, et éventuellement substitué par un radical (C₁-C₄) alkyle, préférentiellement méthyle ;
  • un radical amino substitué par un ou deux radicaux alkyle, identiques ou différents, en C₁-C₆ éventuellement porteurs d'au moins :
    1. i) un groupe hydroxy,
    2. ii) un groupe amino éventuellement substituté par un ou deux radicaux alkyle en C₁-C₃ éventuellement substitués, lesdits radicaux alkyle pouvant former avec l'atome d'azote auquel ils sont rattachés, un hétérocycle comprenant de 5 à 7 chaînons, saturé ou insaturé éventuellement substitué comprenant éventuellement au moins un autre hétéroatome différent ou non de l'azote,
  • -NR-COR' dans lequel le radical R est un atome d'hydrogène, un radical alkyle en C₁-C₄ éventuellement porteur d'au moins un groupe hydroxy et le radical R' est un radical alkyle en C₁-C₂ ;
  • (R)₂N-CO- dans lequel les radicaux R, identiques ou non, représentent un atome d'hydrogène, un radical alkyle en C₁-C₄ éventuellement porteur d'au moins un groupe hydroxy ;
  • R'SO₂-NR- dans lequel le radical R représente un atome d'hydrogène, un radical alkyle en C₁-C₄ éventuellement porteur d'au moins un groupe hydroxy et le radical R' représente un radical alkyle en C₁-C₄, un radical phényle ;
  • (R)₂N-SO₂- dans lequel les radicaux R, identiques ou non, représentent un atome d'hydrogène, un radical alkyle en C₁-C₄ éventuellement porteur d'au moins un groupe hydroxy,
  • un radical carboxylique sous forme acide ou salifiée (de préférence avec un métal alcalin ou un ammonium, substitué ou non) ;
  • un groupe cyano ;
  • un groupe polyhalogénoalkyle comprenant de 1 à 6 atomes de carbones et de 1 à 6 atome d'halogène, identiques ou différents, le groupe polyhalogénoalkyle est par exemple le trifluorométhyle ;
• la partie cyclique ou hétérocyclique d'un radical non aromatique peut être substituée par au moins un substituant porté par un atome de carbone choisi parmi les groupes :
  • hydroxy,
  • alcoxy en C₁-C₄,
  • (poly)hydroxyalcoxy en C₂-C₄,
  • un radical alkylthio en C₁-C₂ ;
  • RCO-NR'- dans lequel le radical R' est un atome d'hydrogène, un radical alkyle en C₁-C₄ éventuellement porteur d'au moins un groupe hydroxy et le radical R est un radical alkyle en C₁-C₂, amino substitué par deux groupes alkyle identiques ou différents en C₁-C₄ éventuellement porteurs d'au moins un groupe hydroxy ;
  • RCO-O- dans lequel le radical R est un radical alkyle en C₁-C₄, amino substitué par un ou deux groupes alkyle identiques ou différents en C₁-C₄ éventuellement porteurs d'au moins un groupe hydroxy, lesdits radicaux alkyle pouvant former avec l'atome d'azote auquel ils sont rattachés, un hétérocycle comprenant de 5 à 7 chaînons, saturé ou insaturé éventuellement substitué comprenant éventuellement au moins un autre hétéroatome différent ou non de l'azote ;
  • RO-CO- dans lequel le radical R est un radical alkyle en C₁-C₄ éventuellement porteurs d'au moins un groupe hydroxy ;
• un radical cyclique, hétérocyclique, ou une partie non aromatique d'un radical aryle ou hétéroaryle, peut également être substitué par un ou plusieurs groupes oxo ou thioxo ;
• un radical « aryle » représente un groupe carboné mono ou polycyclique, condensé ou non, comprenant de 6 à 22 atomes de carbones, et dont au moins un cycle est aromatique ; préférentiellement le radical aryle est un phényle, biphényle, naphtyle, indényle, anthracényle, ou tétrahydronaphtyle ;
• un radical « diarylalkyle » représente un groupe comportant sur le même atome de carbone d'un groupe alkyle deux groupe aryle, identiques ou différents tel que diphénylméthyle ou 1,1-diphényléthyle ;
• un « radical hétéroaryle » représente un groupe mono ou polycyclique, condensé ou non, éventuellement cationique, comprenant de 5 à 22 chaînons, de 1 à 6 hétéroatomes choisis parmi l'atome d'azote, d'oxygène, de soufre et de sélénium, et dont au moins un cycle est aromatique ; préférentiellement un radical hétéroaryle est choisis parmi acridinyle, benzimidazolyle, benzobistriazolyle, benzopyrazolyle, benzopyridazinyle, benzoquinolyle, benzothiazolyle, benzotriazolyle, benzoxazolyle, pyridinyle, tétrazolyle, dihydrothiazolyle, imidazopyridinyle, imidazolyle, indolyle, isoquinolyle, naphthoimidazolyle, naphthooxazolyle, naphthopyrazolyle, oxadiazolyle, oxazolyle, oxazolopyridyle, phénazinyle, phénooxazolyle, pyrazinyle, pyrazolyle, pyrilyle, pyrazoyltriazyle, pyridyle, pyridinoimidazolyle, pyrrolyle, quinolyle, tétrazolyle, thiadiazolyle, thiazolyle, thiazolopyridinyle, thiazoylimidazolyle, thiopyrylyle, triazolyle, xanthylyle et son sel d'ammonium ;
• un radical « dihétéroarylalkyle » représente un groupe comportant sur le même atome de carbone d'un groupe alkyle deux groupe hétéroaryle, identiques ou différents tel que difurylméthyle, 1,1-difuryléthyle, dipyrrolylméthyle, dithiénylméthyle ;
• un « radical cyclique » est un radical cycloalkyle non aromatique, mono ou polycyclique, condensé ou non, contenant de 5 à 22 atomes de carbone, pouvant comporter de 1 à plusieurs insaturations ; particulièrement le radical cyclique est un cyclohexyle ;
• un radical « cyclique stériquement encombré» est un radical cyclique, aromatique ou non, substitué ou non, encombré par effet ou contrainte stérique, comprenant de 6 à 14 chaînons, pouvant être pontés, à titre de radicaux stériquement encombrés on peut citer le bicyclo[1.1.0]butane, les mésytyles tels que le 1,3,5-triméthylpnényle, le 1,3,5-triterbutylphényle, le 1,3,5-isobutylphényle, le 1,3,5-trimétylsillylphényle et l'adamantyle ;
• un « radical hétérocyclique ou hétérocycle» est un radical non aromatique mono ou polycyclique, condensé ou non, contenant de 5 à 22 chaînons, comportant de 1 à 6 hétéroatomes choisis parmi l'atome d'azote, d'oxygène, de soufre et de sélénium, particulièrement le radical est monocyclique, contient de 5 à 7 chaînons et 1 ou 2 hétéroatomes choisis parmi l'azote, l'oxygène et le soufre, dont au moins un des hétéroatome est un atome d'azote ; plus particulièrement le radical hétérocyclique est choisi parmi pyrrolidinyle, et pipéridyle ;
• un « radical alkyle » est un radical hydrocarboné en C₁-C₁₆, linéaire ou ramifié, de préférence en C₁-C₈ ;
• l'expression « éventuellement substitué » attribué au radical alkyle sous entend que ledit radical alkyle peut être substitué par un ou plusieurs radicaux choisis parmi les radicaux i) hydroxy, ii) alcoxy en C₁-C₄, iii) acylamino, iv) amino éventuellement substitué par un ou deux radicaux alkyle, identiques ou différents, en C₁-C₄, lesdits radicaux alkyles pouvant former avec l'atome d'azote qui les portent un hétérocyle comprenant de 5 à 7 chaînons, comprenant éventuellement un autre hétéroatome différent ou non de l'azote ; v) ou un groupe ammonium quaternaire -N⁺R'R''R''', M^-pour lequel R', R", R"', identiques ou différents représentent un atome d'hydrogène, ou un groupe alkyle en C₁-C₄, ou alors -N⁺R'R"R"' forme un hétéroaryle tel que imidazolium éventuellement substitué par un groupe C₁-C₄ alkyle, et M représente le contre-ion de l'acide organique, minéral ou de l'halogénure correspondant,
• un « radical alcoxy » est un radical alkyle-oxy ou alkyl-O- pour lequel le radical alkyle est un radical hydrocarboné, linéaire ou ramifié, en C₁-C₁₆ préférentiellement en C₁-C₈ ;
• un « radical alkylthio » est un radical alkyl-S- pour lequel le radical alkyle est un radical hydrocarboné, linéaire ou ramifié, en C₁-C₁₆ préférentiellement en C₁-C₈ ; lorsque le groupe alkylthio est éventuellement substitué, cela sous entend que le groupe alkyle est éventuellement substitué tel que défini précédemment ;
• les bornes délimitant l'étendue d'une plage de valeurs sont comprises dans cette plage de valeurs ;
• un « sel d'acide organique ou minéral » est plus particulièrement choisi parmi un sel dérivé i) d'acide chlorhydrique HCl, ii) d'acide bromhydrique HBr, iii) d'acide sulfurique H₂SO₄, iv) d'acides alkylsulfoniques : Alk-S(O)₂OH tels que d'acide méthylsulfonique et d'acide éthylsulfonique ; v) d'acides arylsulfoniques : Ar-S(O)₂OH tel que d'acide benzène sulfonique et d'acide toluène sulfonique ; vi) d'acide citrique ; vii) d'acide succinique ; viii) d'acide tartrique ; ix) d'acide lactique, x) d'acides alkoxysulfiniques : Alk-O-S(O)OH tels que d'acide méthoxysulfinique et d'acide éthoxysulfinique ; xi) d'acides aryloxysulfiniques tels que d'acide toluèneoxysulfinique et d'acide phénoxysulfinique ; xii) d'acide phosphorique H₃PO₄; xiii) d'acide acétique CH₃COOH ; xiv) d'acide triflique CF₃SO₃H et xv) d'acide tétrafluoroborique HBF₄ ;
• un « contre-ion anionique » est un anion ou un groupe anionique associé à la charge cationique du colorant ; plus particulièrement le contre-ion anionique est choisi parmi i) les halogénures tels que le chlorure, le bromure ; ii) les nitrates ; iii) les sulfonates parmi lesquels les C₁-C₆ alkylsulfonates : Alk-S(O)₂O^- tels que le méthylsulfonate ou mésylate et l'éthylsulfonate ; iv) les arylsulfonates : Ar-S(O)₂O^- tel que le benzènesulfonate et le toluènesulfonate ou tosylate ; v) le citrate ; vi) le succinate ; vii) le tartrate ; viii) le lactate ; ix) les alkylsulfates : Alk-O-S(O)O^- tels que le méthysulfate et l'éthylsulfate ; x) les arylsulfates : Ar-O-S(O)O^- tels que le benzènesulfate et le toluènesulfate ; xi) les alkoxysulfates : Alk-O-S(O)₂O^- tel que le méthoxy sulfate et l'éthoxysulfate ; xii) les aryloxysulfates : Ar-O-S(O)₂O^-, xiii) le phosphate ; xiv) l'acétate ; xv) le triflate ; et xvi) les borates tels que le tétrafluoroborate ;
• les « solvates » représentent les hydrates ainsi que l'association avec des alcools linéaires ou ramifiés en C1-C4 linéaire ou ramifié tels que l'éthanol, l'isopropanol, le n-propanol.

For the purposes of the present invention, and unless a different indication is given:

• the "aryl" or "heteroaryl" radicals or the aryl or heteroaryl part of a radical may be substituted by at least one substituent carried by a carbon atom chosen from:
  • an alkyl radical C ₁ -C _16, preferably C ₁ -C _8, optionally substituted by one or more radicals chosen from hydroxyl, alkoxy, C ₁ -C ₂ alkyl, (poly) hydroxyalkoxy, C ₂ -C ₄ , acylamino, amino substituted with two identical or different C ₁ -C ₄ alkyl radicals, optionally carrying at least one hydroxyl group, or the two radicals being able to form, with the nitrogen atom to which they are attached, a 5- to 7-membered, preferably 5 or 6-membered, optionally substituted saturated or unsaturated heterocycle optionally comprising another heteroatom which is the same or different from nitrogen;
  • a halogen atom such as chlorine, fluorine or bromine;
  • a hydroxy group;
  • a C ₁ -C ₂ alkoxy radical;
  • a C ₁ -C ₂ alkylthio radical;
  • a (C ₂ -C ₄ ) polyhydroxyalkoxy radical;
  • an amino radical;
  • a 5- or 6-membered heterocycloalkyl radical;
  • a 5- or 6-membered optionally cationic heteroaryl radical, preferentially imidazolium, and optionally substituted with a (C ₁ -C ₄ ) alkyl radical, preferably methyl;
  • an amino radical substituted with one or two identical or different C ₁ -C ₆ alkyl radicals optionally carrying at least:
    1. i) a hydroxy group,
    2. ii) an amino group optionally substituted with one or two optionally substituted C ₁ -C ₃ alkyl radicals, said alkyl radicals being able to form, with the nitrogen atom to which they are attached, a 5- to 7-membered heterocycle, saturated or optionally substituted unsaturated optionally comprising at least one other heteroatom different or different from nitrogen,
  • -NR-COR 'in which the radical R is a hydrogen atom, a C ₁ -C ₄ alkyl radical optionally bearing at least one hydroxyl group and the radical R' is a C ₁ -C ₂ alkyl radical; ;
  • (R) ₂ N-CO- in which the radicals R, which may be identical or different, represent a hydrogen atom, a C ₁ -C ₄ alkyl radical optionally carrying at least one hydroxyl group;
  • R'SO ₂ -NR- wherein the radical R represents a hydrogen atom, an alkyl radical in C ₁ -C ₄ alkyl optionally bearing at least one hydroxy group and R 'is an alkyl radical C ₁ - C ₄ , a phenyl radical;
  • (R) ₂ N-SO ₂ - in which the radicals R, which may be identical or different, represent a hydrogen atom, a C ₁ -C ₄ alkyl radical optionally carrying at least one hydroxyl group,
  • a carboxylic radical in acid or salified form (preferably with an alkali metal or an ammonium, substituted or unsubstituted);
  • a cyano group;
  • a polyhaloalkyl group comprising from 1 to 6 carbon atoms and from 1 to 6 halogen atoms, which are identical or different, the polyhaloalkyl group is, for example, trifluoromethyl;
• the cyclic or heterocyclic part of a nonaromatic radical may be substituted by at least one substituent carried by a carbon atom chosen from the groups:
  • hydroxy,
  • C ₁ -C ₄ alkoxy,
  • (poly) hydroxyalkoxy C ₂ -C ₄ ,
  • a C ₁ -C ₂ alkylthio radical;
  • RCO-NR'- in which the radical R 'is a hydrogen atom, a C ₁ -C ₄ alkyl radical optionally bearing at least one hydroxyl group and the radical R is a C ₁ -C ₂ alkyl radical; amino substituted with two identical or different C ₁ -C ₄ alkyl groups optionally bearing at least one hydroxyl group;
  • RCO-O- wherein the radical R is a C ₁ -C ₄ alkyl radical, amino substituted with one or two identical or different C ₁ -C ₄ alkyl groups optionally carrying at least one hydroxyl group, said alkyl radicals capable of forming, with the nitrogen atom to which they are attached, a 5- to 7-membered optionally substituted saturated or unsaturated heterocycle optionally comprising at least one other heteroatom which is different from or different from nitrogen;
  • RO-CO- wherein the radical R is a C ₁ -C ₄ alkyl radical optionally carrying at least one hydroxyl group;
• a cyclic, heterocyclic, or nonaromatic portion of an aryl or heteroaryl radical may also be substituted by one or more oxo or thioxo groups;
• an "aryl" radical represents a mono or polycyclic carbon group, condensed or not, comprising from 6 to 22 carbon atoms, and of which at least one ring is aromatic; preferably the aryl radical is a phenyl, biphenyl, naphthyl, indenyl, anthracenyl, or tetrahydronaphthyl;
• a "diarylalkyl" radical represents a group comprising, on the same carbon atom of an alkyl group two aryl groups, identical or different such as diphenylmethyl or 1,1-diphenylethyl;
• a "heteroaryl radical" represents a mono or polycyclic group, condensed or not, optionally cationic, comprising from 5 to 22 members, from 1 to 6 heteroatoms chosen from nitrogen, oxygen, sulfur and selenium, and wherein at least one ring is aromatic; preferably heteroaryl is selected from acridinyl, benzimidazolyl, benzobistriazolyl, benzopyrazolyl, benzopyridazinyle, benzoquinolyl, benzothiazolyl, benzotriazolyl, benzoxazolyl, pyridinyl, tetrazolyl, dihydrothiazolyl, imidazopyridinyl, imidazolyl, indolyl, isoquinolyl, naphthoimidazolyle, naphthooxazolyle, naphthopyrazolyle, oxadiazolyl, oxazolyl, oxazolopyridyl phenazinyl, phenoxazolyl, pyrazinyl, pyrazolyl, pyrilyl, pyrazoyltriazyl, pyridyl, pyridinoimidazolyl, pyrrolyl, quinolyl, tetrazolyl, thiadiazolyl, thiazolyl, thiazolopyridinyl, thiazoylimidazolyl, thiopyrylyl, triazolyl, xanthylyl and its ammonium salt;
• a "diheteroarylalkyl" radical represents a group comprising, on the same carbon atom of a two or more heteroaryl alkyl group, identical or different, such as difurylmethyl, 1,1-difurylethyl, dipyrrolylmethyl, dithienylmethyl;
• a "cyclic radical" is a non-aromatic, mono- or polycyclic cycloalkyl radical, condensed or not, containing from 5 to 22 carbon atoms, which may contain from 1 to several unsaturations; particularly the cyclic radical is cyclohexyl;
• a "sterically hindered cyclic" radical is a cyclic radical, aromatic or not, substituted or unsubstituted, hindered by steric effect or constraint, comprising from 6 to 14 members, which can be bridged, as sterically hindered radicals, mention may be made of bicyclo [ 1.1.0] butane, mesylates such as 1,3,5-trimethylphenyl, 1,3,5-triterbutylphenyl, 1,3,5-isobutylphenyl, 1,3,5-trimethylsillylphenyl and adamantyl;
• a "heterocyclic radical or heterocycle" is a non-aromatic radical, mono or polycyclic, condensed or not, containing from 5 to 22 members, comprising from 1 to 6 heteroatoms chosen from nitrogen, oxygen, sulfur and selenium, especially the radical is monocyclic, contains 5 to 7 members and 1 or 2 heteroatoms selected from nitrogen, oxygen and sulfur, wherein at least one of the heteroatoms is a nitrogen atom; more particularly the heterocyclic radical is chosen from pyrrolidinyl and piperidyl;
• an "alkyl radical" is a linear or branched C ₁ -C ₁₆ hydrocarbon radical, preferably a C ₁ -C ₈ hydrocarbon radical;
• the term "optionally substituted" ascribed to the alkyl radical implies that said alkyl radical may be substituted by one or more radicals chosen from the radicals i) hydroxy, ii) alkoxy C ₁ -C ₄ , iii) acylamino, iv) amino optionally substituted with one or two identical or different C ₁ -C ₄ alkyl radicals, said alkyl radicals being capable of forming, with the nitrogen atom carrying them, a 5- to 7-membered heterocyl, optionally comprising another different heteroatom; or not nitrogen; v) or a quaternary ammonium group -N ⁺ R'R''R ''', M ^- for which R', R ", R"', which may be identical or different, represent a hydrogen atom, or a C 1 -alkyl group; ₁ -C ₄ , or -N ⁺ R'R "R"'forms a heteroaryl such as imidazolium optionally substituted with a C ₁ -C ₄ alkyl group, and M represents the counterion of the organic acid, mineral or the corresponding halide,
• an "alkoxy radical" is an alkyl-oxy or alkyl-O- radical for which the alkyl radical is a hydrocarbon radical, linear or branched, in C ₁ -C ₁₆ preferentially in C ₁ -C ₈ ;
• an "alkylthio radical" is an alkyl-S- radical for which the alkyl radical is a hydrocarbon radical, linear or branched, C ₁ -C ₁₆ preferably C ₁ -C ₈ ; when the alkylthio group is optionally substituted, this implies that the alkyl group is optionally substituted as defined above;
• the bounds defining the range of a range of values lie within this range of values;
• an "organic or inorganic acid salt" is more particularly chosen from a salt derived from i) hydrochloric acid HCl, ii) hydrobromic acid HBr, iii) sulfuric acid H ₂ SO ₄ , iv) acids alkylsulfonic: Alk-S (O) ₂ OH such as methylsulfonic acid and ethylsulfonic acid; v) arylsulfonic acids: Ar-S (O) ₂ OH such as benzene sulfonic acid and toluene sulfonic acid; (vi) citric acid; vii) succinic acid; viii) tartaric acid; ix) lactic acid, x) alkoxysulfinic acids: Alk-OS (O) OH such as methoxysulfinic acid and ethoxysulfinic acid; xi) aryloxysulfinic acids such as tolueneoxysulfinic acid and phenoxysulfinic acid; xii) phosphoric acid H ₃ PO ₄ ; xiii) acetic acid CH ₃ COOH; xiv) triflic acid CF ₃ SO ₃ H and xv) tetrafluoroboric acid HBF ₄ ;
• an "anionic counterion" is an anion or an anionic group associated with the cationic charge of the dye; more particularly the anionic counterion is selected from i) halides such as chloride, bromide; ii) nitrates; iii) sulfonates, including C ₁ -C ₆ alkylsulphonates: Alk-S (O) ₂ O ^- such as methylsulfonate or mesylate and ethylsulfonate; iv) arylsulfonates: Ar-S (O) ₂ O ^- such as benzenesulfonate and toluenesulphonate or tosylate; v) citrate; vi) succinate; (vii) tartrate; viii) lactate; ix) alkyl sulphates: Alk-OS (O) O ^- such as methysulfate and ethylsulfate; x) arylsulfates: Ar-OS (O) O ^- such as benzenesulphate and toluenesulphate; xi) Alkoxysulfates: Alk-OS (O) ₂ O ^- such as methoxy sulfate and ethoxysulfate; xii) aryloxysulfates: Ar-OS (O) ₂ O ^-, xiii) phosphate; (xiv) acetate; xv) triflate; and xvi) borates such as tetrafluoroborate;
• the "solvates" represent the hydrates as well as the association with linear or branched C1-C4 linear or branched alcohols such as ethanol, isopropanol and n-propanol.

One of the objects of the invention relates to thiol / disulfide fluorescent dyes of formula (I) .

The thiol / disulfide fluorescent dyes of formula (I) are compounds capable of absorbing in UV or visible radiation at a wavelength λ _abs of between 250 and 800 nm and capable of reemitting in the visible range to a length emission wave λ _em between 400 and 800 nm.

Preferably, the fluorescent compounds of formula (I) of the invention are dyes capable of absorbing in the visible λ _abs between 400 and 800 nm and reemitting in the visible λ _em between 400 and 800 nm. More preferentially, the dyes of formula (I) are dyes capable of absorbing at an λ _abs of between 420 nm and 550 nm and of reemitting in the visible at an λ _em of between 470 and 600 nm.

The thiol fluorescent compounds of the invention of formula (I) for which m and n are 1, contain a SY function which may be in the covalent -SY or ionic -S ^- Y ^{+ form} depending on the nature of Y and the pH middle.

When the compounds of the invention contain several ions against anionic An ^-, against said ions may be the same or different.

One particular mode relates to thiol fluorescent dyes of formula (II) for which m and n are 1, with SY function where Y represents a hydrogen atom, or an alkali metal. Advantageously, Y represents a hydrogen atom.

According to another particular embodiment of the invention, in formula (I) above, Y is a protecting group known to those skilled in the art such as those described in the books "Protective Groups in Organic Synthesis", TW Greene, John Willey & Sons ed., NY, 1981, pp.193-217 ; "Protecting Groups", P. Kocienski, Thieme, 3rd ed., 2005, chap. 5 . It being understood that Y, as a protecting group, can not constitute with the sulfur atom to which it is attached a disulfide dye ie not be a formula (I) in which m = 2 and n = 0. Y as a protecting group can not represent a group directly attached to the sulfur atom of formula (I) via another nonoxidized sulfur atom.

• ■ (C₁-C₄)alkylcarbonyle ;
• ■ (C₁-C₄)alkylthiocarbonyle ;
• ■ (C₁-C₄)alcoxycarbonyle ;
• ■ (C₁-C₄)alcoxythiocarbonyle ;
• ■ (C₁-C₄)alkylthio-thiocarbonyle ;
• ■ (di)(C₁-C₄)(alkyl)aminocarbonyle ;
• ■ (di)(C₁-C₄)(alkyl)aminothiocarbonyle;
• ■ arylcarbonyle comme phénylcarbonyle ;
• ■ aryloxycarbonyle ;
• ■ aryl(C₁-C₄)alkcoxycarbonyle ;
• ■ (di)(C₁-C₄)(alkyl)aminocarbonyle comme diméthylaminocarbonyle ;
• ■ (C₁-C₄)(alkyl)arylaminocarbonyle ;
• ■ carboxy ;
• ■ SO₃ ^-; M⁺ avec M⁺ représentant un métal alcalin tel que le sodium ou le potassium, ou alors An^- de la formule (I) et M⁺ sont absents ;
• ■ aryle éventuellement substitué tel que le phényle, dibenzosubéryle, ou 1,3,5-cycloheptatriényle,
• ■ hétéroaryle éventuellement substitué ; dont notamment l'hétéroaryle cationiques ou non, comprenant de 1 à 4 hétéroatomes suivants :
  1. i) monocycliques à 5, 6 ou 7 chaînons tels que furanyle ou furyle, pyrrolyle ou pyrryle, thiophényle ou thiényle, pyrazolyle, oxazolyle, oxazolium, isoxazolyle, isoxazolium, thiazolyle, thiazolium, isothiazolyle, isothiazolium, 1,2,4-triazolyle, 1,2,4-triazolium, 1,2,3-triazolyle, 1,2,3-triazolium, 1,2,4-oxazolyle, 1,2,4-oxazolium, 1,2,4-thiadiazolyle, 1,2,4-thiadiazolium, pyrylium, thiopyridyle, pyridinium, pyrimidinyle, pyrimidinium, pyrazinyle, pyrazinium, pyridazinyle, pyridazinium, triazinyle, triazinium, tétrazinyle, tétrazinium, azépine, azépinium, oxazépinyle, oxazépinium, thiépinyle, thiépinium, imidazolyle, imidazolium ;
  2. ii) bicycliques à 8 à 11 chaînons tels que indolyle, indolinium, benzoimidazolyle, benzoimidazolium, benzoxazolyle, benzoxazolium, dihydrobenzoxazolinyle, benzothiazolyle, benzothiazolium, pyridoimidazolyle, pyridoimidazolium, thiénocycloheptadiényle, ces groupes mono ou bicycliques étant éventuellement substitués par un ou plusieurs groupes tels que (C₁-C₄)alkyle comme méthyle, ou polyhalogéno(C₁-C₄)alkyle comme trifluorométhyle ;
  3. iii) ou tricyclique ABC suivant :
     

dans lequel les deux cycles A, C comportent éventuellement un hétéroatome, et le cycle B est un cycle à 5, 6 ou 7 chaînons particulièrement à 6 chaînons et contient au moins un hétéroatome comme pypéridyle, pyranyle ;

• ■ hétérocycloalkyle éventuellement substitué, éventuellement cationique, le groupe hétérocycloalkyle représente notamment un groupe monocyclique saturé ou partiellement saturé à 5, 6 ou 7 chaînons comprenant de 1 à 4 hétéroatomes choisis parmi l'oxygène, le soufre et l'azote, tel que di/tétrahydrofuranyle, di/tétrahydrothiophényle, di/tétrahydropyrrolyle, di/tétrahydropyranyle, di/tétra/hexahydrothiopyranyle, dihydropyridyle, pipérazinyle, pipéridinyle, tétraméthylpipéridinyle, morpholinyle, di/tétra/hexahydroazépinyle, di/tétrahydropyrimidinyle ces groupes étant éventuellement substitués par un ou plusieurs groupes comme (C₁-C₄)alkyle, oxo ou thioxo ; ou l'hétérocycle représente le groupe suivant :
  

dans lequel R'^c, R'^d, R'^e, R'^f, R'^g et R'^h, identiques ou différents représentent un atome d'hydrogène ou un groupe (C₁-C₄)alkyle, ou alors deux groupe R'^g avec R'^h, et/ou R'^e avec R'^f forment un groupe oxo ou thioxo, ou alors R'^g avec R'^e forment ensemble un cycloalkyle ; et v représente un entier compris inclusivement entre 1 et 3 ; préférentiellement R'^c à R'^h représentent un atome d'hydrogène ; et An'^- représente un contre-ion anionique;

• ■ isothiouronium ;
• ■ -C(NR'^cR'^d)=N⁺R'^eR'^f; An^- avec R'^c, R'^d, R'^e et R'^f, identiques ou différents représentent un atome d'hydrogène ou un groupe (C₁-C₄)alkyle ; préférentiellement R'^c à R'^f représentent un atome d'hydrogène ; et An'^-représente un contre-ion anionique;
• ■ isothiourée ;
• ■ -C(NR'^cR'^d)=NR'^e; An^- avec R'^c, R'^d, R'^e et An^- sont tels que définis précédemment ;
• ■ (di)aryl(C₁-C₄)alkyle éventuellement substitué tel que le 9-anthracénylméthyle, phénylméthyle ou diphénylméthyle éventuellement substitué par un plusieurs groupes notamment choisis parmi (C₁-C₄) alkyle, (C₁-C₄) alcoxy comme le méthoxy, hydroxy, alkylcarbonyle, (di)(C₁-C₄)(alkyl)amino comme le diméthylamino ;
• ■ (di)hétéroaryl(C₁-C₄)akyle éventuellement substitué, le groupe hétéroaryle est notamment, cationique ou non, monocyclique, comprenant 5 ou 6 chaînons et de 1 à 4 hétéroatomes choisis parmi l'azote, l'oxygène et le soufre, tels que les groupes pyrrolyle, furanyle, thiophényle, pyridyle, pyridyle N-oxyde tels que le 4-pyridyle ou 2-pyridyl-N-oxyde, pyrylium, pyridinium, triazinyle, éventuellement substitué par un ou plusieurs groupe tel que alkyle particulièrement méthyle, avantageusement le (di)hétéroaryl(C₁-C₄)akyle est (di)hétéroarylméthyle ou (di)hétéroaryléthyle ;
• ■ -CR¹R²R³ avec R¹, R² et R³ identiques ou différents, représentant un atome d'halogène ou un groupe choisi parmi :
  1. i) (C₁-C₄)alkyle ;
  2. ii) (C₁-C₄)alcoxy ;
  3. iii) aryle éventuellement substitué tel que phényle éventuellement substitué par un ou plusieurs groupes comme (C₁-C₄)alkyle, (C₁-C₄)alcoxy, hydroxy ;
  4. iv) hétéroaryle éventuellement substitué tel que thiophényle, furanyle, pyrrolyle, pyranyle, pyridyle, éventuellement substitué par un groupe (C₁-C₄)alkyle ;
  5. v) P(Z¹)R'¹R'²R'³ avec R'¹, et R'² identiques ou différents représentent un groupe hydroxy, (C₁-C₄)alcoxy ou alkyle, R'³ représente un groupe hydroxy ou (C₁-C₄)alcoxy, et Z¹ représente un atome d'oxygène ou de soufre ;
• ■ cyclique stériquement encombré ; et
• ■ alcoxyalkyle éventuellement substitué tels que le méthoxyméthyle (MOM), éthoxyéthyle (EOM) et l'isobutoxyméthyle.

Especially when Y represents a protecting group of the thiol function, Y is chosen from the following radicals:

• (C ₁ -C ₄ ) alkylcarbonyl;
• (C ₁ -C ₄ ) alkylthiocarbonyl;
• (C ₁ -C ₄ ) alkoxycarbonyl;
• (C ₁ -C ₄ ) alkoxythiocarbonyl;
• (C ₁ -C ₄ ) alkylthiothiocarbonyl;
• ■ (di) (C ₁ -C ₄ ) (alkyl) aminocarbonyl;
• ■ (di) (C ₁ -C ₄ ) (alkyl) aminothiocarbonyl;
• Arylcarbonyl such as phenylcarbonyl;
• Aryloxycarbonyl;
• Aryl (C ₁ -C ₄ ) alkoxycarbonyl;
• (Di) (C ₁ -C ₄ ) (alkyl) aminocarbonyl as dimethylaminocarbonyl;
• (C ₁ -C ₄ ) (alkyl) arylaminocarbonyl;
• ■ carboxy;
• ■ SO ₃ ^- ; M ⁺ with M ⁺ representing an alkali metal such as sodium or potassium, or then An ^- of the formula (I) and M ⁺ are absent;
• Optionally substituted aryl such as phenyl, dibenzosuberyl, or 1,3,5-cycloheptatrienyl,
• Optionally substituted heteroaryl; of which in particular cationic or non-cationic heteroaryl, comprising from 1 to 4 following heteroatoms:
  1. i) 5, 6 or 7 membered monocyclic such as furanyl or furyl, pyrrolyl or pyrryl, thiophenyl or thienyl, pyrazolyl, oxazolyl, oxazolium, isoxazolyl, isoxazolium, thiazolyl, thiazolium, isothiazolyl, isothiazolium, 1,2,4-triazolyl, 1,2,4-triazolium, 1,2,3-triazolyl, 1,2,3-triazolium, 1,2,4-oxazolyl, 1,2,4-oxazolium, 1,2,4-thiadiazolyl, 1, 2,4-thiadiazolium, pyrylium, thiopyridyl, pyridinium, pyrimidinyl, pyrimidinium, pyrazinyl, pyrazinium, pyridazinyl, pyridazinium, triazinyl, triazinium, tetrazinyl, tetrazinium, azepine, azepinium, oxazepinyl, oxazepinium, thiepinyl, thiepinium, imidazolyl, imidazolium;
  2. ii) 8 to 11-membered bicyclics such as indolyl, indolinium, benzoimidazolyl, benzoimidazolium, benzoxazolyl, benzoxazolium, dihydrobenzoxazolinyl, benzothiazolyl, benzothiazolium, pyridoimidazolyl, pyridoimidazolium, thienocycloheptadienyl, these mono or bicyclic groups being optionally substituted with one or more groups such as (C ₁ -C ₄ ) alkyl as methyl, or polyhalo (C ₁ -C ₄ ) alkyl as trifluoromethyl ;
  3. iii) or tricyclic ABC following:
     

wherein the two rings A, C optionally comprise a heteroatom, and the ring B is a 5-, 6- or 7-membered particularly 6-membered ring and contains at least one heteroatom such as pyperidyl, pyranyl;

• Optionally substituted heterocycloalkyl, optionally cationic heterocycloalkyl represents in particular a saturated or partially saturated 5, 6 or 7 membered monocyclic group comprising from 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen, such as di / tetrahydrofuranyl, di / tetrahydrothiophenyl, di / tetrahydropyrrolyl, di / tetrahydropyranyl, di / tetra / hexahydrothiopyranyl, dihydropyridyl, piperazinyl, piperidinyl, tetramethylpiperidinyl, morpholinyl, di / tetra / hexahydroazepinyl, di / tetrahydropyrimidinyl these groups being optionally substituted with one or more groups such as (C ₁ -C ₄ ) alkyl, oxo or thioxo; or the heterocycle represents the following group:
  

wherein R ^'c, R' ^d, R ^e, R ^f, R ^g and R ^h are identical or different represent a hydrogen atom or a (C ₁ -C ₄₎ alkyl, or else two R ' ^g with R' ^h , and / or R ' ^e with R' ^f form an oxo or thioxo group, or R ' ^g with R' ^e together form a cycloalkyl; and v represents an integer inclusive of between 1 and 3; preferentially R ' ^c to R' ^h represent a hydrogen atom; and An ' ^- represents an anionic counterion;

• ■ isothiouronium;
• -C (NR ' ^c R' ^d ) = N ⁺ R ' ^e R'^f; An ^- with R ^'c, R' ^d, R ^'e and R' ^f, like or different, represent a hydrogen atom or a (C ₁ -C ₄₎ alkyl; preferably R ' ^c to R' ^f represent a hydrogen atom; and An ' ^- represents an anionic counterion;
• ■ isothiourea;
• -C (NR ' ^c R' ^d ) = NR '^e; An ^- with R ' ^c , R' ^d , R ' ^e and An ^- are as defined previously;
• Optionally substituted (di) aryl (C ₁ -C ₄ ) alkyl, such as 9-anthracenylmethyl, phenylmethyl or diphenylmethyl, optionally substituted with one or more groups chosen in particular from (C ₁ -C ₄ ) alkyl, (C ₁ -C ₄ ) alkoxy such as methoxy, hydroxy, alkylcarbonyl, (di) (C ₁ -C ₄ ) (alkyl) amino such as dimethylamino;
• (Di) heteroaryl (C ₁ -C ₄ ) alkyl optionally substituted, the heteroaryl group is in particular, cationic or non-monocyclic, comprising 5 or 6 members and 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur, such as pyrrolyl, furanyl, thiophenyl, pyridyl, pyridyl N-oxide such as 4-pyridyl or 2-pyridyl-N-oxide, pyrylium, pyridinium, triazinyl, optionally substituted by one or more group such as alkyl particularly methyl, advantageously (di) heteroaryl (C ₁ -C ₄ ) alkyl is (di) heteroarylmethyl or (di) heteroarylethyl;
• -CR ¹ R ² R ³ with R ¹ , R ² and R ^{3, which may be} identical or different, representing a halogen atom or a group chosen from:
  1. i) (C ₁ -C ₄ ) alkyl;
  2. ii) (C ₁ -C ₄ ) alkoxy;
  3. iii) optionally substituted aryl such as phenyl optionally substituted with one or more groups such as (C ₁ -C ₄ ) alkyl, (C ₁ -C ₄ ) alkoxy, hydroxy;
  4. iv) optionally substituted heteroaryl such as thiophenyl, furanyl, pyrrolyl, pyranyl, pyridyl, optionally substituted with a (C ₁ -C ₄ ) alkyl group;
  5. v) P (Z ¹ ) R ' ¹ R' ² R ' ³ with R' ¹ , and R ' ^{2, which may be} identical or different, represent a hydroxyl, (C ₁ -C ₄ ) alkoxy or alkyl group, R' ³ represents a group hydroxy or (C ₁ -C ₄ ) alkoxy, and Z ¹ represents an oxygen or sulfur atom;
• Cyclic sterically hindered; and
• Optionally substituted alkoxyalkyl such as methoxymethyl (MOM), ethoxyethyl (EOM) and isobutoxymethyl.

dans lequel R'^c et R'^d, identiques ou différents, représentent un atome d'hydrogène ou un groupe (C₁-C₄)alkyle ; préférentiellement R'^c à R'^d représentent un groupe (C₁-C₄)alkyle tel que méthyle ; et An'^- représente un contre-ion anionique.According to a particular embodiment, the protected thiol fluorescent dyes of formula (I) for which m and n are equal to 1 contain a group Y i) cationic aromatic 5- or 6-membered monocyclic heteroaryl comprising from 1 to 4 heteroatoms chosen from oxygen , sulfur and nitrogen, such as oxazolium, isoxazolium, thiazolium, isothiazolium, 1,2,4-triazolium, 1,2,3-triazolium, 1,2,4-oxazolium, 1,2,4-thiadiazolium, pyrylium, pyridinium, pyrimidinium, pyrazinyl, pyrazinium, pyridazinium, triazinium, tetrazinium, oxazepinium, thiepinyl, thiepinium, imidazolium; ii) cationic 8 to 11-membered bicyclic heteroaryl such as indolinium, benzoimidazolium, benzoxazolium, benzothiazolium, these mono or bicyclic heteroaryl groups being optionally substituted by one or more groups such as alkyl as methyl, or polyhalo (C ₁ -C ₄ ) alkyl as trifluoromethyl; iii) or heterocyclic according to:

in which R ' ^c and R' ^d , identical or different, represent a hydrogen atom or a (C ₁ -C ₄ ) alkyl group; preferentially R ' ^c to R' ^d represent a (C ₁ -C ₄ ) alkyl group such as methyl; and An ' ^- represents an anionic counterion.

• ➢ (C₁-C₄)alkylcarbonyle comme méthylcarbonyle ou éthylcarbonyle ;
• ➢ arylcarbonyle comme phénylcarbonyle ;
• ➢ (C₁-C₄)alkoxycarbonyle ;
• ➢ aryloxycarbonyle ;
• ➢ aryl(C₁-C₄)alkoxycarbonyle ;
• ➢ (di)(C₁-C₄)(alkyl)aminocarbonyle comme diméthylaminocarbonyle;
• ➢ (C₁-C₄)(alkyl)arylaminocarbonyle ;
• ➢ aryle éventuellement substitué tel que le phényle ;
• ➢ hétéroaryle monocyclique à 5 ou 6 chaînons tels que imidazolyle ou pyridyle ;
• ➢ hétéroaryle monocyclique cationique à 5, 6 chaînons tels que pyrylium, pyridinium, pyrimidinium, pyrazinium, pyridazinium, triazinium, imidazolium ; ces groupes étant éventuellement substitués par un ou plusieurs, identiques ou différents, groupes (C₁-C₄)alkyle tel que méthyle ;
• ➢ hétéroaryle bicyclique cationique à 8 à 11 chaînons tels que benzoimidazolium, ou le benzoxazolium ; ces groupes étant éventuellement substitué par un ou plusieurs, identiques ou différents, groupes (C₁-C₄)alkyle tel que méthyle ;
• ➢ hétérocycle cationique de formule suivante :
  
• ➢ isothiouronium -C(NH₂)=N⁺H₂; An^-;
• ➢ isothiourée -C(NH₂)=NH ;
• ➢ SO₃ ^-, M⁺ avec M⁺ représentant un métal alcalin tel que le sodium ou le potassium, ou alors An^- de la formule (I) et M⁺ sont absents.

Especially Y represents a group selected from oxazolium, isoxazolium, thiazolium, isothiazolium, 1,2,4-triazolium, 1,2,3-triazolium, 1,2,4-oxazolium, 1,2,4-thiadiazolium, pyrylium, pyridinium , pyrimidinium, pyrazinium, pyridazinium, triazinium and imidazolium, benzoimidazolium, benzoxazolium, benzothiazolium, these groups being optionally substituted by one or more (C ₁ -C ₄ ) alkyl groups including methyl. In particular, Y represents an alkali metal or a protective group such as:

• (C ₁ -C ₄ ) alkylcarbonyl such as methylcarbonyl or ethylcarbonyl;
• Arylcarbonyl as phenylcarbonyl;
• (C ₁ -C ₄ ) alkoxycarbonyl;
• Aryloxycarbonyl;
• Aryl (C ₁ -C ₄ ) alkoxycarbonyl;
• (Di) (C ₁ -C ₄ ) (alkyl) aminocarbonyl as dimethylaminocarbonyl;
• (C ₁ -C ₄ ) (alkyl) arylaminocarbonyl;
• Optionally substituted aryl such as phenyl;
• 5- or 6-membered monocyclic heteroaryl such as imidazolyl or pyridyl;
• Cationic monocyclic 5- to 6-membered heteroaryl such as pyrylium, pyridinium, pyrimidinium, pyrazinium, pyridazinium, triazinium, imidazolium; these groups being optionally substituted by one or more, identical or different, (C ₁ -C ₄ ) alkyl groups such as methyl;
• 8 to 11-membered cationic bicyclic heteroaryl such as benzoimidazolium, or benzoxazolium; these groups being optionally substituted by one or more, identical or different, (C ₁ -C ₄ ) alkyl groups such as methyl;
• Cationic heterocycle of following formula:
  
• ➢ isothiouronium -C (NH ₂ ) = N ⁺ H ₂ ; An ^- ;
• ➢ isothiourea -C (NH ₂ ) = NH;
• ➢ SO ₃ ^- , M ⁺ with M ⁺ representing an alkali metal such as sodium or potassium, or then An ^- of the formula (I) and M ⁺ are absent.

According to a particular embodiment of the invention, the disulfide fluorescent dyes of formula (I) when n is 2 and m is 0 have an axis of symmetry C2 between the two sulfur atoms of the central disulfide radical.

leurs sels d'acide organique ou minéral, isomères optiques, isomères géométriques, et les solvates tels que hydrates ; formules (Ia) et (Ib) avec :

• R'₁ , représente un groupe alkyle en C₁-C₄ substitué par un ou plusieurs groupes hydroxyle, particulièrement par un seul groupe hydroxyle ou -C(O)OR' avec R' représentant un atome d'hydrogène, un groupe alkyle en C₁-C₄ ou alors un groupe - C(O)-O^- et dans ce dernier cas un contre ion anionique An^- est absent;
• R'₂ , représente un groupe alkyle en C₁-C₄ éventuellement substitué par un ou plusieurs groupes hydroxyle ; particulièrement par un seul groupe hydroxyle ; plus particulièrement R'₁ et R'₂ sont identiques ;
• R'₃ , et R'₄ , identiques ou différents, représentent un atome d'hydrogène, un groupe hydroxyle, un groupe hydroxy(C₁-C₄)alkyle ou -C(O)OR' avec R' représentant un atome d'hydrogène, un groupe alkyle en C₁-C₄ ou alors un groupe -C(O)-O^- et dans ce cas un contre ion anionique An^- est absent, étant entendu qu'un seul de ces deux radicaux R'₃ ou R'₄ ne peuvent représenter un atome d'hydrogène ;
• R₃ représente un atome d'hydrogène ou un groupement -C(O)OR" avec R" représentant un atome d'hydrogène, un groupe alkyle en C₁-C₄ ou alors R₃ représente un groupe -C(O)-O^- et dans ce cas un contre ion anionique An^- est absent ;
• n vaut 1 ou 2 ;
• m vaut 0 ou 1 ;
• t vaut 1 ou 2 ;
• An^- représente un contre ion anionique ;
• Y représente : i) un atome d'hydrogène ; ii) un métal alcalin ; iii) un métal alcalino-terreux ; iv) un groupe ammonium : N⁺R^αR^βR^γR^δ, An^- ou un groupe phosphonium : P⁺R^αR^βR^γR^δ, An^- avec R^α, R^β, R^γ et R^δ, identiques ou différents, représentant un atome d'hydrogène ou un groupe (C₁-C₄)alkyle et An^- est tels que défini précédemment ; ou v) un groupe protecteur de fonction thiol ; étant entendu que :
  • la liaison entre le cycle pyridinium et la double liaison du groupe styryle est positionnée en position 2 ou 4 du pyridinium ;
  • lorsque n=1, m=1 alors Y = H ou groupe protecteur de la fonction thiol et lorsque n=2, alors m=0.

According to one particular embodiment of the invention, the dyes of the invention belong to one of the following two formulas (Ia) or (Ib) :

their organic or inorganic acid salts, optical isomers, geometric isomers, and solvates such as hydrates; formulas (Ia) and (Ib) with:

• R ' ₁ , represents a C ₁ -C ₄ alkyl group substituted by one or more hydroxyl groups, particularly by a single hydroxyl group or -C (O) OR' with R 'representing a hydrogen atom, an alkyl group or C ₁ -C ₄ or a group - C (O) -O ^- and in this case an anionic counterion An ^- is absent;
• R ' ₂ represents a C ₁ -C ₄ alkyl group optionally substituted with one or more hydroxyl groups; particularly by a single hydroxyl group; more particularly R ' ₁ and R' ₂ are identical;
• R ' ₃ and R' ₄ , which may be identical or different, represent a hydrogen atom, a hydroxyl group, a hydroxy (C ₁ -C ₄ ) alkyl group or -C (O) OR 'with R' representing a hydrogen atom; hydrogen, a C ₁ -C ₄ alkyl group or a -C (O) -O ^{- group} and in this case anionic counterion An ^- is absent, it being understood that only one of these two radicals R ' ₃ or R' ₄ can not represent a hydrogen atom;
• R ₃ represents a hydrogen atom or a group -C (O) OR "with R" representing a hydrogen atom or a C ₁ -C ₄ alkyl group or R ₃ represents a -C (O) - group O ^- and in this case an anionic counter ion An ^- is absent;
• n is 1 or 2;
• m is 0 or 1;
• t is 1 or 2;
• An ^- represents anionic counterion;
• Y represents: i) a hydrogen atom; ii) an alkali metal; iii) an alkaline earth metal; iv) an ammonium group: N ⁺ R ^α R ^β R ^γ R ^δ , An ^- or a phosphonium group: P ⁺ R ^α R ^β R ^γ R ^δ , An ^- with R ^α , R ^β , R ^γ and R ^δ , identical or different, representing a hydrogen atom or a group (C ₁ -C ₄ ) alkyl and An ^- is as defined above; or v) a thiol protecting group; Being heard that :
  • the bond between the pyridinium ring and the double bond of the styryl group is positioned in position 2 or 4 of the pyridinium;
  • when n = 1, m = 1 then Y = H or protecting group of the thiol function and when n = 2, then m = 0.

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To prepare thiol / disulfide fluorescent dyes according to the invention, one can cite the following general routes.

Protected thiol dyes of formula (II ') can be synthesized in two stages. The first step of preparing the unprotected thiol dye (II ") according to methods known to those skilled in the art, for example Thiols and organic Sulfides, Thiocyanates and Isothiocyanates, organic, Ullmann's Encyclopedia, Wiley-VCH, Weinheim, 2005 . And the second step of protecting the thiol function according to conventional methods known to those skilled in the art to lead to protected thiol dyes of formula (II ') . By way of example, to protect the thiol -SH function of the thiol dye, the methods of the structures can be used "Protective Groups in Organic Synthesis", TW Greene, John Willey & Sons ed., NY, 1981, pp.193-217 ; "Protecting Groups", P. Kocienski, Thieme, 3rd ed., 2005, chap. 5 .

avec Y' représentant un groupe protecteur de fonction thiol ; Met* représentant un métal alcalin ou un métal alcalino térreux, particulièrement le sodium ou le potassium, étant entendu que lorsque le métal est un métal alcalino-terreux 2 chromophores à fonction thiolate-S^- peuvent être associés à 1 Métal²⁺. avec R₁, R₂, R₃, R₄, m, n, G et An^- sont tels que définis précédemment ; Y' représente un groupe protecteur de fonction thiol ; et R représente un groupe partant nucléofuge, comme par exemple mésylate, tosylate, triflate ou halogénure.We can illustrate this method by the method consisting of i) generating thiol fluorescent dyes of formula (II ") by reduction of a heterophylic, heterocyclic fluorescent dye bearing a disulfide -SS- function such as (I ') and ii) to protect according to conventional methods said thiol function of (II ") with the reagent 7 Y'R to access the protected thiol fluorescent dyes of formula (II ') . The thiol compound (II ") may also be metallized with an alkali metal or alkaline earth metal Met * to yield the thiolate fluorescent dye of formula (II ''') .

with Y 'representing a thiol protecting group; Met * represents an alkali metal or an alkaline earth metal, particularly sodium or potassium, it being understood that when the metal is an alkaline earth metal 2 thiolate-functional chromophores-S ^- may be associated with 1 Metal ²⁺ . with R ₁ , R ₂ , R ₃ , R ₄ , m, n, G and An ^- are as defined above; Y 'represents a protecting group of thiol function; and R represents a leaving group nucleofuge, such as, for example, mesylate, tosylate, triflate or halide.

avec R₁, R₂, Y' et An^- sont tels que définis précédemment ; R'₁, R'₂, R'₃, R'₄ représentant des chaînes alkyles en C₁-C₄ éventuellement substituées par un groupement acide carboxylique, un sel d'acide carboxylique, une fonction ester, ou un groupement hydrogène, m et n entiers compris entre 1 et 4, Nu représentant un groupe nucléophile de type amine ; E représentant un groupe électrophile; et Σ le groupe de liaison générée après attaque du nucléophile sur l'électrophile.According to another possibility, a protected thiol compound (b) can be reacted with a protective group Y 'as defined previously prepared according to one of the procedures described in the works cited above, said protected thiol compound comprising at least one nucleophilic function with a a sufficient amount, preferably equimolar, of a "reactive fluorescent chromophore" or a compound comprising such a "reactive fluorescent chromophore" (a) . In other words (a) comprises an electrophilic function for forming a covalent bond Σ as can be schematized below in the preparation of fluorescent dyes of formula (II'a) , sub-set of fluorescent dyes (II '):

with R ₁ , R ₂ , Y 'and An ^- are as defined above; R ' ₁ , R' ₂ , R ' ₃ , R' ₄ representing C ₁ -C ₄ alkyl chains optionally substituted by a carboxylic acid group, a carboxylic acid salt, an ester function, or a hydrogen group, m and n integers between 1 and 4, Nu representing a nucleophilic group of amine type; E representing an electrophilic group; and Σ the linking group generated after nucleophilic attack on the electrophile.

By way of example, the bonds that can be generated are listed in the table below from the condensation of electrophiles with nucleophiles: Electrophiles E Nucleophiles Naked Covalent bonds Σ Esters activated * amines carboxamides Acyl azides amines carboxamides Acyl halogenation amines carboxamides Acyl cyanides amines carboxamides anhydrides amines carboxamides Carboxylic acids amines carboxamides * activated esters of general formula -CO-Part with Part representing a leaving group such as oxysuccinimidyl, oxybenzotriazolyl, optionally substituted aryloxy;

avec R₁, R₂, R₃, Z, Y', (II') et An^- sont tels que définis précédemment, et Hal représentant un atome d'halogène nucléofuge tel que le brome, l'iode ou le chlore.It is also possible to use a thiol reagent (α) : Y'-SH comprising a group Y 'as defined previously, whose nucleophilic function SH can react on the carbon atom alpha of the halogen atom carried by a chromophore fluorescent to lead to the protected thiol fluorescent dye of formula (II ') :

with R ₁ , R ₂ , R ₃ , Z, Y ', (II') and An ^- are as defined above, and Hal represents a nucleofugal halogen atom such as bromine, iodine or chlorine.

avec R₁, R₂, R₃, Z, Hal et An sont tels que définis précédemment, R'_c et R'_d représentant des groupements alkyles en C₁-C_4; (II"") représentant un colorant sous ensemble de la formule (II') More particularly, a nucleofugal leaving group may be substituted with a group derived from thiourea (S = C (NRR) NRR) or thiourea to generate isothiouroniums. For example, if the thiourea group is a thioimidazolium (β) , the reaction scheme is as follows:

with R ₁ , R ₂ , R ₃ , Z, Hal and An are as defined above, R ' _c and R' _d representing C ₁ -C ₄ alkyl groups _; (II "") representing a dye under a set of formula (II ')

avec R₁, R₂, R₃, Z, R'_c, R'_d, (II'), Hal et An-, sont tels que définis précédemment.Another variant may make it possible to access certain compounds (II ') from cyclic thiourea of imidazoline type ( b ') , followed by the alkylation of said imidazoline using R ' _d -Gp with Gp group. starting material such as chloride, bromide, tosylate, mesylate:

with R _1, R _2, R _3, Z, R _'c, R' _d, (II), Hal and An- are as defined above.

An alternative is to use in place of the halide comprising the fluorescent chromophore (a ') a chromophore comprising another type of nucleofuge such as tosylate mesylate.

avec R₁, R₂, R'_c, R'_d, An-, R'₁, R'₂, R'₃, R'₄, Y', m, n, E, Nu et (II'a) tels que définis précédemment.According to another possibility, certain protected thiols fluorescent dyes (II'a) can be obtained by reacting a protected thiol compound with a compound carrying an activated carboxylic acid function according to conventional methods (for example reaction with a carbodiimide or with thionyl chloride). The resulting product (d) is then reacted with a fluorescent chromophore carrying a nucleophilic function (c) , primary or secondary amine type.

with R _1, R _2, R _'c, R' _d, An-, R _'1, R' _2, R _'3, R' _4, Y ', m, n, E, and Nu (II'a) as defined previously.

Another variant is to use a thiolactone derivative as represented by the scheme below:

With R ₁ , R ₂ , R ' ₁ , R' ₂ Y ', Met *, m, n An ^- , as defined above. The thiolactone derivative is preferentially chosen with n = 3.

A synthetic variant is to combine the first route, ie from two equivalents of the nucleophilic reagent (c) with a disulfide dielectrophile reactant (i). It is possible to generate the dichromophoric disulfide product (I) after condensation. the latter can be reduced to form the heterocyclic fluorescent thiol dye (II "a) which in turn can either be protected to form the protected thiol fluorescent dye (II'a) or be metallized with an alkali metal to yield the fluorescent dye metallocyclic heterocyclic thiol (II '''a) :

Avec R₁, R₂, R₃, Z, Y', , (II') et sont tels que définis précédemment.According to another possibility, the protected thiol fluorescent dyes of formula (II ') can be obtained by reaction of a compound having a thiol group protected by a group Y', and a leaving group Gp, such as a grouping halogens (chlorine, bromine) or a previously activated hydroxy group in nucleofugal leaving group such as, for example, mesylate, tosylate, triflate or halide with a styrylpyridine chromophore (c ') .

With R ₁ , R ₂ , R ₃ , Z, Y ', (II') and are as defined above.

avec R₁, R₂, R₃, Z, Y' An^- tels que définis précédemment et G' représentant un atome d'oxygène ou de soufre.According to another possibility, the thiol fluorescent dyes of formula (I) according to the invention can be obtained by reaction of a compound comprising a group thiol protected by a group Y as defined above and an electrophilic group (f) with a pyridinium compound comprising a nucleophilic group. By way of example, an aldehyde or a thioaldehyde may be condensed when G 'represents an oxygen atom or a sulfur with an "activated methylene" such as alkylpyridinium (e) to generate an ethylene bond> C = C < . This reaction is commonly known as "Knoevenagel" condensation. By "activated methylenes" is meant those having in position 2 or 4 of the pyridinium group a methylene group CH ₃ -:

with R ₁ , R ₂ , R ₃ , Z, Y 'An ^- as defined above and G' representing an oxygen or sulfur atom.

We can refer to the book Advanced Organic Chemistry, "Reactions, Mechanisms and Structures," J. March, 4th Ed, John Willey & Sons, 1992 or TW Greene "Protective Groups in Organic Synthesis" , for more details on the operating conditions used for the processes mentioned above.

The thiol fluorescent dyes formed can be converted to protected thiol stain -SY 'by protecting the thiol -SH using conventional protecting groups. The thiol fluorescent dyes are metallated using also the conventional methods known to those skilled in the art such as those described in US Pat. Advanced Organic Chemistry, "Reactions, Mechanisms and Structures," J. March, 4th Ed, John Willey & Sons, NY, 1992 .

Protected thiol dyes can be deprotected by conventional routes such as those described in the literature "Protective Groups in Organic Synthesis," TW Greene, John Willey & Sons ed., NY, 1981 ; "Protecting Groups", P. Kocienski, Thieme, 3rd ed., 2005 .

avec Gp représentant un groupe partant nucléofuge, comme par exemple mésylate, tosylate, triflate ou halogénure. Les contre-ions Gp^- des composés (I'), ci-dessus peuvent être remplacés par des contre-ions An^- d'autres natures à partir de méthodes connues par l'homme du métier notamment par résine échangeuse d'ion.The starting reagents are commercial or accessible by conventional methods known to those skilled in the art. By way of example, it is possible to synthesize the reagent (I ') from 2 equivalents of pyridine derivative 1 and one equivalent of disulfide reagent comprising two leaving groups Gp, to give the dipyridinium disulfide salt 3 which can condense on turn with two equivalents of aryl compound to aldehyde / thioaldehyde group 4 to yield 5.

with Gp representing a leaving group nucleofuge, such as mesylate, tosylate, triflate or halide. The counter ions Gp ^- compounds (I ') , above may be replaced by counter-ions An ^- other natures from methods known to those skilled in the art including ion exchange resin.

We can refer to the book Advanced Organic Chemistry, "Reactions, Mechanisms and Structures," J. March, 4th Ed, John Willey & Sons, 1992 or TW Greene "Protective Groups in Organic Synthesis" , for more details on the operating conditions used for the processes mentioned above.

The thiol fluorescent dyes formed can be converted to protected thiol stain -SY 'by protecting the thiol -SH using conventional protecting groups. The thiol fluorescent dyes are metallated using also the conventional methods known to those skilled in the art such as those described in US Pat. Advanced Organic Chemistry, "Reactions, Mechanisms and Structures," J. March, 4th Ed, John Willey & Sons, NY, 1992 .

Protected thiol dyes can be deprotected by conventional routes such as those described in the literature "Protective Groups in Organic Synthesis," TW Greene, John Willey & Sons ed., NY, 1981 ; "Protecting Groups", P. Kocienski, Thieme, 3rd ed., 2005 .

Another subject of the invention relates to a dyeing composition for dyeing keratin materials which contains at least one thiol / disulfide fluorescent dye of formula (I) . In addition to the presence of at least one fluorescent dye of formula (I), the composition of the invention may also contain a reducing agent.

This reducing agent may be chosen from thiols, for example cysteine, homocysteine, thiolactic acid, the salts of these thiols, phosphines, bisulphite, sulphites, thioglycolic acid, and its esters, in particular glycerol monothioglycolate, and thioglycerol. This reducing agent may also be chosen from borohydrides and their derivatives, such as, for example, borohydride, cyanoborohydride, triacetoxyborohydride or trimethoxyborohydride salts: sodium, lithium, potassium, calcium, quaternary ammonium salts (tetramethylammonium, tetraethylammonium, tetra butylammonium, benzyltriethylammonium); catechol borane.

The dye composition useful in the invention generally contains a quantity of fluorescent dye of formula (I) of between 0.001% and 50% relative to the total weight of the composition. Preferably, this amount is between 0.005 and 20% by weight and even more preferably between 0.01 and 5% by weight relative to the total weight of the composition.

The dye composition may further contain additional direct dyes. These direct dyes are, for example, chosen from neutral, acidic or cationic nitro-benzene direct dyes, neutral azo, acid or cationic direct dyes, tetraazapentamethine dyes, neutral or acidic or cationic quinone dyes, in particular neutral anthraquinone dyes and direct azine dyes. , triarylmethane direct dyes, indoamine direct dyes and natural direct dyes.

Among the natural direct dyes that may be mentioned are lawsone, juglone, alizarin, purpurin, carminic acid, kermesic acid, purpurogalline, protocatechaldehyde, indigo, isatin, curcumin, spinulosin, apigenidine. It is also possible to use the extracts or decoctions containing these natural dyes, and in particular poultices or extracts made from henna.

The dye composition may contain one or more oxidation bases and / or one or more couplers conventionally used for dyeing keratinous fibers.

Among the oxidation bases that may be mentioned are para-phenylenediamines, bis-phenylalkylenediamines, para-aminophenols, bis-para-aminophenols, ortho-aminophenols, heterocyclic bases and their addition salts.

Among these couplers, there may be mentioned meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalenic couplers, heterocyclic couplers and their addition salts.

The coupler or couplers are each generally present in an amount of between 0.001 and 10% by weight of the total weight of the dye composition, preferably between 0.005 and 6%.

The oxidation base (s) present in the dyeing composition are in general present each in an amount of between 0.001% and 10% by weight relative to the total weight of the dye composition, preferably between 0.005 and 6% by weight.

In general, the addition salts of the oxidation bases and couplers that can be used in the context of the invention are chosen especially from the addition salts with an acid such as hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates and addition salts with a base such as alkali metal hydroxides such as sodium hydroxide, potassium hydroxide, ammonia, amines or alkanolamines.

The medium suitable for dyeing, also called dyeing medium, is a cosmetic medium generally consisting of water or a mixture of water and at least one organic solvent. Examples of organic solvents that may be mentioned are lower C ₁ -C ₄ alkanols, such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether and monomethyl ether, as well as aromatic alcohols such as benzyl alcohol or phenoxyethanol, and mixtures thereof.

The solvents other than water when they are present are preferably present in proportions preferably of between 1 and 40% by weight approximately relative to the total weight of the dye composition, and even more preferably between 5 and 30% by weight approx. The solvents including water are present, preferably present in proportions preferably of between 1 and 99% by weight approximately relative to the total weight of the dye composition, and even more preferably between 5 and 95% by weight approximately.

According to one variant, the composition of the invention contains a reducing agent capable of reducing the disulfide bonds of the keratin and / or disulphide of the fluorescent dyes of formula (I). This reducing agent is as defined above.

The dye composition may also contain various adjuvants conventionally used in compositions for dyeing hair, such as anionic, cationic, nonionic, amphoteric, zwitterionic surfactants or mixtures thereof, anionic, cationic, nonionic, amphoteric and zwitterionic polymers. or mixtures thereof, inorganic or organic thickeners, and in particular anionic, cationic, nonionic and amphoteric polymeric associative thickeners, antioxidants, penetrating agents, sequestering agents, perfumes, buffers, dispersing agents, conditioning agents such as, for example, volatile or non-volatile silicones, modified or otherwise, such as aminosilicones, film-forming agents, ceramides, preserving agents, opacifying agents, conductive polymers.

The adjuvants above are generally present in an amount included for each of them between 0.01 and 20% by weight relative to the weight of the composition.

Of course, one skilled in the art will take care to choose this or these optional additional compounds in such a way that the advantageous properties intrinsically attached to the dyeing composition according to the invention are not, or not substantially, impaired by the or the additions envisaged.

The pH of the dyeing composition is generally between 3 and 14 approximately, and preferably between 5 and 11 approximately. It can be adjusted to the desired value by means of acidifying or alkalizing agents usually used for dyeing keratin fibers or else using conventional buffer systems.

Among the acidifying agents, mention may be made, by way of example, of mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids such as acetic acid, tartaric acid, citric acid, lactic acid, sulphonic acids.

dans laquelle W_a est un reste propylène éventuellement substitué par un groupe hydroxy ou un radical alkyle en C₁-C₄ ; R_a1, R_a2, R_a3 et R_a4, identiques ou différents, représentent un atome d'hydrogène, un radical alkyle en C₁-C₄ ou hydroxyalkyle en C₁-C₄.Among the alkalinizing agents that may be mentioned, by way of example, are ammonia, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamines and their derivatives, sodium or potassium hydroxides and following formula (γ):

wherein W _a is a propylene residue optionally substituted by a hydroxy group or a C ₁ -C ₄ alkyl radical; R _a1, R _a2, R _a3 and R _a4, identical or different, represent a hydrogen atom, an alkyl radical in C ₁ -C ₄ hydroxyalkyl or C ₁ -C _4.

The dye composition may be in various forms, such as in the form of liquid, cream, gel, or in any other form suitable for dyeing keratinous fibers, and in particular hair.

Another subject of the invention is a method for dyeing keratinous material comprising applying to said materials a composition comprising at least one dye of formula (I). According to a particular embodiment in the method of the invention, a reducing agent may also be applied as a pre-treatment before the application of the composition containing at least one fluorescent dye of formula (I).

This reducing agent may be chosen from thiols, for example cysteine, homocysteine, thiolactic acid, the salts of these thiols, phosphines, bisulfite, sulphites, thioglycolic acid and its esters, especially the glycerol monothioglycolate, and thioglycerol. This reducing agent may also be chosen from borohydrides and their derivatives, such as, for example, borohydride, cyanoborohydride, triacetoxyborohydride or trimethoxyborohydride salts: sodium, lithium, potassium, calcium, quaternary ammonium salts (tetramethylammonium, tetraethylammonium, tetra-n-butylammonium, benzyltriethylammonium); catecholborane.

This pretreatment may be of short duration, especially from 1 second to 30 minutes, preferably from 1 minute to 15 minutes with a reducing agent as mentioned above.

According to another method, the composition comprising at least one fluorescent dye of formula (I) and also contains at least one reducing agent as defined above. This composition is then applied to the hair.

When the thiol fluorescent dye of formula (I) with n = m = 1 comprises a group Y protecting the thiol function, the process of the invention may be preceded by a deprotection step aimed at restoring the SH function in situ .

For example, it is possible to deprotect the SY function with Y protecting group by adjusting the pH as follows: Y: protective group protection alkylcarbonyl, pH> 9 arylcarbonyl, pH> 9 alkoxycarbonyl, pH> 9 aryloxycarbonyl, pH> 9 aralkoxycarbonyl pH> 9 (Di) (alkyl) aminocarbonyl, pH> 9 (Alkyl) arylaminocarbonyl pH> 9 optionally substituted aryl such as phenyl, pH> 9 5-, 6-, or 7-membered monocyclic heteroaryl such as oxazolium; pH> 9 8 to 11-membered bicyclic heteroaryl such as benzoimidazolium, or benzoxazolium pH> 9

The deprotection step may also be carried out during a hair pretreatment step such as, for example, the hair reduction pretreatment.

According to one variant, the reducing agent is added to the dyeing composition containing at least one fluorescent dye of formula (I) at the time of use.

According to another method, the composition comprising at least one fluorescent dye of Formula (I) also contains at least one reducing agent as defined above. This composition is then applied to the hair.

According to another variant, the reducing agent is applied in post-treatment, after the application of the composition containing at least one fluorescent dye of formula (I). The duration of the post-treatment with the reducing agent may be short, for example from 1 second to 30 minutes, preferably from 1 minute to 15 minutes, with a reducing agent as described above. According to a particular embodiment, the reducing agent is a thiol or borohydride type agent as described above.

A particular embodiment of the invention relates to a process in which the fluorescent dye of formula (I) can be applied directly to hair without reducing agents, free of pre or post-treatment reducers.

A treatment with an oxidizing agent may optionally be associated. Any type of conventional oxidizing agent may be used in the art. Thus, it may be chosen from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, as well as the enzymes among which may be mentioned peroxidases, oxides, 2-electron reductases such as uricases and 4-electron oxygenases such as laccases. The use of hydrogen peroxide is particularly preferred.

This oxidizing agent may be applied to the fibers before or after the application of the composition containing at least one fluorescent dye of formula (I). A particular embodiment of the invention relates to the method of the invention comprising an additional step which consists in applying to the keratin fibers an oxidizing agent.

The application of the dye composition according to the invention is generally carried out at room temperature. It can however be carried out at temperatures ranging from 20 to 180 ° C.

The invention also relates to a multi-compartment device or "kit" of dyeing in which a first compartment contains a dye composition comprising at least one fluorescent dye of formula (I) and a second compartment contains a reducing agent capable of reducing disulfide functions of the keratin materials and / or disulfide fluorescent dye of formula (I), when n is 2 and m is 0.

One of these compartments may further contain one or more other dyes of direct dye type or oxidation dye.

It also relates to a multi-compartment device in which a first compartment contains a dye composition comprising at least one fluorescent dye of formula (I); a second compartment contains a reducing agent capable to reduce the disulfide bond of the keratin materials and / or the disulfide fluorescent dye of formula (I) when n is 2 and m is 0; a third compartment contains an oxidizing agent.

Alternatively, the dyeing device contains a first compartment containing a dye composition which comprises at least one protected thiol fluorescent dye of formula (I) when n = m = 1 and a second compartment containing an agent capable of deprotecting the protected thiol to release the thiol.

Each of the devices mentioned above may be equipped with a means for delivering the desired mixture onto the hair, for example such as the devices described in the patent. FR2 586 913 .

The examples which follow serve to illustrate the invention without, however, being limiting in nature. The thiol fluorescent dyes of the examples below have been fully characterized by conventional spectroscopic and spectrometric methods.

EXAMPLES EXAMPLES OF SYNTHESIS Example 1 Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (2-oxoethane-2,1-diyl)]} bis [4 - (- 2- {4- [bis (2) dichloride -hydroxyethyl) amino] phenyl} vinyl) pyridinium]

Step 1: Synthesis of N, N '- (disulfanediyldiethane-2,1-diyl) bis (2-chloroacetamide)

40.3 g of cystamine dihydrochloride are dissolved in 100 ml of water, 32 ml of 35% sodium hydroxide are added (pH 9.7) and the temperature is lowered to 5 °. 33.5 ml of chloroacetyl chloride are introduced dropwise, keeping the temperature below 10 ° C and maintaining the pH between 7.9 and 9.3 by adding sodium hydroxide. The medium is kept stirred at room temperature for 2 h. The precipitate is filtered, washed with 5 × 150 ml of water and then dried under vacuum in the presence of P ₂ O ₅ . 35.3 g of white powder are collected. the analyzes indicate that the product is compliant.

Step 2: Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (2-oxoethane-2,1-diyl)]} bis (4-methylpyridinium) dichloride

6.1 g N, N '- (disulfanediyldiethane-2,1-diyl) bis (2-chloroacetamide) and 4.5 g of 4-picoline are dissolved in 50 ml of NMP and brought to 80 ° C for 19 h. After cooling the mixture, by successive precipitation in acetone and drying under vacuum, 9.2 g of salts are collected. The analyzes show that the product is compliant. ¹ H NMR (400 MHz, D ₂ O): 2.61 (s, 6H), 2.82 (t, 4H), 3.56 (t, 4H), 5.31 (s, 4H), 7.85 (d, 4H), 8.51 (d, 4H).

Step 3: Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (2-oxoethane-2,1-diyl)]} bis [4- (2- {4- bis-2- dichloride hydroxyethyl) amino] phenyl} vinyl) pyridinium] [1]

837 mg of 4- [bis- (2-hydroxyethyl) amino] benzaldehyde, 328 μl of pyrrolidine, 232 μl of acetic acid and 490 mg of 1,1 '- {disulfanediylbis [ethane-2] dichloride; 1-diylimino (2-oxoethane-2,1-diyl)]} bis (4-methylpyridinium) are dissolved in 10 ml of isopropanol and kept stirred at room temperature for 3 h 30 min. The mixture is poured into 50 ml of 1: 1 dichloromethane / acetone solution. A decanted oil, it is dried under vacuum. 442 mg of black powder are collected. The analyzes show that the product is compliant.

Example 2: 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (2-oxoethane-2,1-diyl)]} bis (4- {2- [4- (3-hydroxypyrrolidin-1-dichloride) yl) phenyl] vinyl} pyridinium)

19.88 g of 4- (3-hydroxypyrrolidin-1-yl) benzaldehyde, 7.17 g of pyrrolidine, 6.05 g of acid acetic acid and 24.8 g of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (2-oxoethane-2,1-diyl)]} bis (4-methylpyridinium) are dissolved in 200 ml of ethanol and kept stirred at room temperature for 48h. The mixture is filtered, washed with 3 times 100 ml of isopropanol. 43.19 g of black powder are collected and then recrystallized from a mixture of 200 mL of ethanol, 50 mL of methanol and 25 mL of water. After filtration and drying under vacuum, 35.8 g of brick red powder are obtained. The analyzes show that the product is compliant.

Example 3 Synthesis of 2,2 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl) pyridinium-1,4-diylethene-2,1-diylbenzene-4.1 diacetate diyl (methylimino)]}

Step 1: Synthesis of N , N '- (disulfanediyldiethane-2,1-diyl) bis (4-chlorobutanamide)

60 g of cystamine hydrochloride are solubilized in 500 ml and cooled to 5 ° C. The pH of 10 is reached by the addition of NaOH (30% aq.). To a solution of 4-chlorobutanoyl chloride (105 g) in anhydrous THF (500 ml) is added dropwise aq. NaOH (30%) so as to maintain the pH around 7. After the reaction is stabilized at pH 7, the mixture is left for 3 days at room temperature. The aqueous phase is extracted with 3 × 500 m of dichloromethane combined with the THF phase and then dried over Na ₂ SO ₄ sodium sulphate. After filtration and drying, 41 g of white powder is collected. The analyzes are in agreement with the expected product.

Step 2: Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl)]} bis (4-methylpyridinium) dichloride

30 g of N, N '- (disulphanediyldiethane-2,1-diyl) bis (4-chlorobutanamide) are dispersed in 100 ml of acetonitrile, 20.2 ml of 4-piolin are added to the reaction mixture with stirring at 80 ° C. for 2 days. After cooling to room temperature, the solvent is evaporated and the resulting oil is washed several times with ethyl acetate. 44.2g of light brown solid are obtained. The analyzes are in agreement with the structure of the expected compound.

Step 3: Synthesis of 2,2 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl) pyridinium-1,4-diylethene-2,1-diylbenzene-4.1 diacetate diyl (methylimino)]}

16.7 g of [(4-formylphenyl) (methyl) amino] acetic acetic acid and 6.3 g of pyrrolidine are mixed in 50 ml of isopropanol at 80 ° C. After 15 min. 1.46 g of pyrrolidine are added followed by the addition of a solution of 22.5 g of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl) dichloride). )]} bis (4-methylpyridinium) in 100 mL of isopropanol. The reaction mixture is heated for 2 hours. then the mixture is cooled to room temperature, then it is poured into 1.4 L of acetone. A precipitate is formed then. The latter is filtered under argon, washed 3 times with 170 mL of acetone and dried. The resulting solid is dispersed in 400 mL of isopropanol and 400 mL of water and 1.2L of acetone are added. The residual oil is dissolved in 50 mL of methanol and 750 mL of acetone is added. A sticky light brown oil is triturated with 500 mL of acetone, filtered and dried. 20.5 g of black powder are collected. The analyzes are consistent with the expected product structure. NMR ¹ H CD ₃ OD ppm: 2.33 (m, 4H), 2.48 (t, 4H), 2.98 (t, 4H), 3.31 (s, 6H), 3.59 (t, 4H), 4.54 (t, 4H), 6.83 (d, 4H), 6.99 (d, 2H), 7.59 (d, 4H) 7.75 (d, 2H), 7.86 (d, 4H), 8.56 (d, 4H).

Example 4 Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl)]} bis {4- [2- {4- [bis- (2) dichloride) hydroxyethyl) amino] phenyl} ethenyl] pyridinium} dichloride

20 g of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl)]} bis (4-methylpyridinium) dichloride, 1.8 ml of piperidine and 16 g of 4- [bis- (2-hydroxyethyl) amino] benzaldehyde are mixed together in 60 ml of isopropanol at 70 ° C. for 18 hours with stirring. After cooling to room temperature the supernatant is removed, the resulting oil is washed 3 times in hot isopropanol (100 mL, 2h at 80 ° C). The oil is diluted in 500 mL of water, iced and lyophilized. 24 g of "flocculent" red powder are collected. The analyzes are consistent with the expected product structure. NMR ¹ H CD ₃ OD ppm: 2.25 (m, 4H), 2.36 (t, 4H), 2.81 (t, 4H), 3.45 (t, 4H), 3.64 (t, 8H), 3.76 (t, 8H), 4.46 (t, 4H), 6.83 (d, 4H), 7.07 (d, 2H), 7.59 (d, 4H), 7.82 (d, 2H), 7.96 (d, 4H), 8.57 (d, 4H), LC / MS gradient ACONH ₄ 20mM-> CH ₃ CN 10min ESI + m / z = 429

Example 5 Synthesis of 2,2 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl) pyridinium-1,2-diylethene-2,1-diylbenzene-4.1 diacetate diyl (methylimino)]}

Step 1: Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl)]} bis (2-methyl-pyridinium) dichloride

1.13 g of N , N '- (disulphanediyldiethane-2,1-diyl) bis (4-chlorobutanamide) are dispersed in 0.5 mL of N-methylpyrrolidinone and 2.5 mL of acetonitrile, and then heated at 50 ° C. 0.71 mL of picoline is then added and the reaction mixture is stirred for 5 days at 50 ° C. A few milligrams of cesium carbonate and 0.35 mL of 2-picoline are added. After 1 day at 65 ° C, the reaction mixture is poured into 50 mL of acetonitrile. The resulting gum is washed several times with ethyl acetate, solubilized in ethanol, filtered and dried under vacuum. 0.95 g of beige solid are collected. The analyzes are in agreement with the structure of the expected compound. LC / MS gradient ACONH ₄ 20mM-> CH ₃ CN 10min ESI + m / z = 238 (dication)

Step 2: Synthesis of 2,2 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl) pyridinium-1,2-diylethene-2,1-diylbenzene-4.1 diacetate diyl (methylimino)]}

0.35 g of [(4-formylphenyl) (methyl) amino] acetic acid, 0.47 g of 1,1 '- {disulfanediylbis- [ethane-2,1-diylimino (4-oxobutane-4,1-diyl) dichloride) ] bis (4-methylpyridinium) and 42 μL of piperidine are mixed in 3 mL of methanol at 70 ° C for 2 h. The reaction mixture is poured into 25 mL of ethyl acetate and the precipitate is filtered and dried. A black powder is obtained. The analyzes are consistent with the expected product structure. LC / MS gradient ACONH ₄ 20mM-> CH ₃ CN 10min ESI + m / z = 413

Example 6 Synthesis of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-diyl)]} bis {2 - [- 2- {4- [bis (2) dichloride -hydroxyethyl) amino] phenyl} ethenyl] pyridinium}

0.37 g of 4- [bis- (2-hydroxy-ethyl) -amino] -benzaldehyde, 0.47 g of 1,1 '- {disulfanediylbis [ethane-2,1-diylimino (4-oxobutane-4,1-) dichloride) diyl)]} bis (4-methylpyridinium) and 42 μl of piperidine are added in 3 mL of methanol at 70 ° C for 2 h. The reaction mixture is poured into 25 mL of ethyl acetate and the precipitate is filtered and dried. A black powder is obtained. The analyzes are consistent with the expected product structure. LC / MS gradient ACONH ₄ 20mM-> CH ₃ CN 10 min ESI + m / z = 429

EXAMPLE OF COLORING Example 1 Coloring Process - Compound [1] Preparation of a composition A

Compound [1] 5x10 ^-4 mol% Benzyl Alcohol 4 g Polyethylene glycol 60E 6 g hydroxyethylcellulose 0.7 g Alkylpolyglucoside in aqueous solution at 65% MA 4.5 g Demineralized Water qsp 100g

Preparation of a composition B

Thioglycolic acid 1M Sodium hydroxide qsp pH 8.5 Demineralized Water qsp 100g

At the time of use, the compositions A (9 ml) and B (1 ml) are mixed, and then the formulas are applied to strands of natural white hair, 90% white (BN), permanent white (BP) or dark hair. of pitch 4 (HT4). The exposure time is 20 minutes at room temperature TA.

After rinsing with running water a fixative (Dulcia Vital II®) diluted by 10 with water is applied for 5 minutes at RT. After rinsing with running water and shampoo, the locks are air-dried. The dark hair thus treated is brightened: the HT4 lock has become visually clearer than untreated control locks. The locks of white hair are colored with intense shades.

Visual observations

During rinsing and shampooing of example [1] there is no visible bleeding, shampoo foam and rinsing water are virtually unstained.

The observed color is conserved on the colored BN and BP and the lightening effect remains visible on shampooed HT4 hair.

Shampoo resistance test

The treated locks are washed by a series of 24 shampoos. It is observed that the foam shampoos is not or very little color and that the color does not fade over time on the locks BN and BP. The lightening effect also remains intact.

Reflectance results for evaluating optical lightening:

The lightening performance of the compositions according to the invention were expressed as a function of the reflectance of the hair. These reflectances are compared to the reflectance of a lock of untreated HT4 pitch hair.

The reflectance is measured using a KONIKA-MINOLTA®, CM 3600d spectrophotocolorimeter and after irradiation of the hair with visible light in the wavelength range of 400 to 700 nanometers.

It is firstly noted that the reflectance of a lock of hair treated with a composition according to the invention is greater than that of untreated hair. In particular, the reflectance of the strands treated with the dye [1] is significantly higher than that of the reference wick in the wavelength range greater than 580 nm. The locks treated with this compound therefore appear clearer. It is also noted that the effect is perfectly preserved after 24 shampoos.

Results in the L * a * b * system to evaluate the color of the locks, BN, BP:

The color of the locks was evaluated in the L * a * b * system using a MINOLTA® CM 3600D spectrocolorimeter (Illuminant D65).

In this system L * a * b *, L * represents the brightness, a * indicates the green / red color axis and b * the blue / yellow color axis. The higher the L value, the lighter or less intense the color. Conversely, the lower the value of L, the darker or more intense the color. The higher the value of a * the higher the shade is red and the higher the value of b * the hue is yellow.

The variation of the coloration between the strands of hair HT4, stained and washed is measured by (ΔE) according to the following equation: $$\mathrm{.DELTA.E}\mathrm{=}\sqrt{{\left({\mathrm{The}}^{\mathrm{*}}\mathrm{-}{{\mathrm{The}}_{\mathrm{o}}}^{\mathrm{*}}\right)}^{\mathrm{2}}\mathrm{+}{\left({\mathrm{at}}^{\mathrm{*}}\mathrm{-}{{\mathrm{at}}_{\mathrm{o}}}^{\mathrm{*}}\right)}^{\mathrm{2}}\mathrm{+}{\left({\mathrm{b}}^{\mathrm{*}}\mathrm{-}{{\mathrm{b}}_{\mathrm{o}}}^{\mathrm{*}}\right)}^{\mathrm{2}}}$$

In this equation, L *, a * and b * represent the values measured before staining and L ₀ *, a ₀ * and b ₀ * represent the measured values before staining (or shampooing).

The higher the value of ΔE, the greater the difference in color between the HT4 and the colored locks is important. L * at* b * of* BN reference 59.9 1.1 11.5 ----- Compound 1 36.3 38.1 23.8 45.6 After 24 shampoos 39.0 37.7 21.9 43.4 BP Reference 58.6 0.7 12.2 ----- Compound 1 32.4 40.8 26.1 49.9 After 24 shampoos 31.8 40.2 23.6 49.1

The natural white and permed white hair is colored bright orange red. The values change very little after the shampoos, given the number of successive shampoos.

Claims (15)

Fluorescent dye of formula (I) :

its organic or inorganic acid salts, optical isomers, geometric isomers, and solvates such as hydrates; formula (I) in which: R ₁ represents a C ₁ -C ₆ alkyl group substituted by one or more hydroxyl groups or -C (O) OR 'with R' representing a hydrogen atom or a C ₁ -C ₄ alkyl group or a -C (O) -O ^{- group} and in the latter case an anionic counterion An ^- is absent; R ₂ represents a C ₁ -C ₆ alkyl group optionally substituted by one or more hydroxyl groups; Or else the groups R ₁ and R ₂ together with the nitrogen atom carrying them form a saturated heterocyclic radical substituted at least by a hydroxyl group, (poly) hydroxy (C ₁ -C ₄ ) alkyl, and or -C (O) OR 'with R' representing a hydrogen atom, a C ₁ -C ₄ alkyl group or a -C (O) -O ^{- group} and in this case an anionic counterion An ^- is absent, R ₃ represents a hydrogen atom or a group -C (O) OR "with R" representing a hydrogen atom, an alkali metal or a C ₁ -C ₆ alkyl group; or when R ₃ is -C (O) O ^- and in this case against an anionic ion An ^- is absent; Z represents a divalent amido group -C (O) -N (R) -, -N (R) -C (O) -, or a divalent C ₁ -C ₁₀ alkylene group interrupted by an amido-C group ( O) -N (R) -, -N (R) -C (O); N is 1 or 2; M is 0 or 1; • An ^- represents anionic counterion; Y represents: i) a hydrogen atom, ii) an alkali metal, iii) an alkaline earth metal, iv) an ammonium group: N ⁺ R ^α R ^β R ^γ R ^δ , a phosphonium group: P ⁺ R ^α R ^β R ^γ R ^δ with R ^α , R ^β , R ^γ and R ^δ , identical or different, representing a hydrogen atom or a (C ₁ -C ₄ ) alkyl group, or v) a functional protective group thiol; Being heard that : the bond between the pyridinium ring and the double bond of the styryl group is positioned at the 2- or 4-position of the pyridinium; when n = 1, m = 1 then Y = H or protecting group of the thiol function and when n = 2, then m = 0; - When the compound of formula (I) contains other cationic parts, it is associated with one or more anionic counter-ions to achieve the electroneutrality of formula (I) . Fluorescent thiol dye of formula (I) according to the preceding claim wherein Y represents a hydrogen atom, or an alkali metal. The thiol fluorescent dye of formula (I) according to claim 1 wherein Y represents a protecting group. Fluorescent thiol dye of formula (I) according to the preceding claim wherein Y represents a protective group chosen from the following radicals: (C ₁ -C ₄ ) alkylcarbonyl; (C ₁ -C ₄ ) alkylthiocarbonyl; (C ₁ -C ₄ ) alkoxycarbonyl; (C ₁ -C ₄ ) alkoxythiocarbonyl; (C ₁ -C ₄ ) alkylthiothiocarbonyl; ■ (di) (C ₁ -C ₄ ) (alkyl) aminocarbonyl; ■ (di) (C ₁ -C ₄ ) (alkyl) aminothiocarbonyl; Arylcarbonyl; Aryloxycarbonyl; Aryl (C ₁ -C ₄ ) alkoxycarbonyl; ■ (di) (C ₁ -C ₄ ) (alkyl) aminocarbonyl; (C ₁ -C ₄ ) (alkyl) arylaminocarbonyl; ■ carboxy; ■ SO ₃ ^- ; M ⁺ with M ⁺ representing an alkali metal or else An ^- of the formula (I) and M ⁺ are absent; Optionally substituted aryl; Optionally substituted heteroaryl; Optionally substituted heterocycloalkyl, optionally cationic, ■ the following group:

wherein R ^'c, R' ^d, R ^e, R ^f, R ^g and R ^h are identical or different represent a hydrogen atom or a (C ₁ -C ₄₎ alkyl, or else two group R ' ^g with R' ^h , and / or R ' ^e with R' ^f form an oxo or thioxo group, or else R ' ^g with R' ^e together form a cycloalkyl; and v represents an integer inclusive of between 1 and 3; preferentially R ' ^c to R' ^h represent a hydrogen atom; and An ' ^- represents an anionic counterion; ■ isothiouronium; -C (NR ' ^c CR _' ^d ) = N + R ' ^e R'f; An ' ^- with R' ^c , R ' ^d , R' ^e and R ' ^f , identical or different, represent a hydrogen atom or a (C ₁ -C ₄ ) alkyl group and An ^- is as defined above; ■ isothiourea; -C (NR ' ^c R' ^d ) = NR '^e; An ' ^- with R' ^c , R ' ^d , R' ^e and An ^- are as defined previously; (Di) aryl (C ₁ -C ₄ ) alkyl optionally substituted; (Di) heteroaryl (C ₁ -C ₄ ) alkyl optionally substituted; -CR ¹ R ² R ³ with R ¹ , R ² and R ^{3, which may be} identical or different, representing a halogen atom or a group chosen from: i) (C ₁ -C ₄ ) alkyl; ii) (C ₁ -C ₄ ) alkoxy; iii) optionally substituted aryl; i) optionally substituted heteroaryl; ii) P (Z ¹ ) R ' ¹ R' ² R ' ³ with R' ¹ , and R ' ^{2 which are} identical or different, represent a hydroxyl, (C ₁ -C ₄ ) alkoxy or alkyl group, R' ³ represents a group hydroxy or (C ₁ -C ₄ ) alkoxy, and Z ¹ represents an oxygen or sulfur atom; Cyclic sterically hindered; and Optionally substituted alkoxyalkyl. A thiol fluorescent dye of formula ( I ) according to any one of the preceding claims wherein Y represents an alkali metal or a protecting group selected from: (C ₁ -C ₄ ) alkylcarbonyl; Arylcarbonyl; (C ₁ -C ₄ ) alkoxycarbonyl; Aryloxycarbonyl; Aryl (C ₁ -C ₄ ) alkoxycarbonyl; (Di) (C ₁ -C _{4 )} (alkyl) aminocarbonyl; (C ₁ -C ₄ ) (alkyl) arylaminocarbonyl; Optionally substituted aryl; 5- or 6-membered cationic monocyclic heteroaryl optionally substituted by one or more, identical or different, (C ₁ -C ₄ ) alkyl groups; 8 to 11-membered cationic bicyclic heteroaryl optionally substituted by one or more, identical or different, (C ₁ -C ₄ ) alkyl groups; Cationic heterocycle of following formula:

➢ isothiouronium; -C (NH ₂ ) = N ⁺ H ₂ ; An '^-; ➢ isothiourea; -C (NH ₂ ) = NH; and ➢ SO ₃ ^- ; M ⁺ with M ⁺ representing an alkali metal or else An ^- of the formula (I) and M ⁺ are absent. Fluorescent disulfide dye according to claim 1 of formula (I) having an axis of symmetry C2 between the two sulfur atoms of the central disulfide radical. Fluorescent dye according to any one of the preceding claims belonging to one of the two formulas (Ia) or (Ib):

its organic or inorganic acid salts, optical isomers, geometric isomers, and solvates such as hydrates; formulas ( Ia ) and (Ib) with: • R _'1 represents an alkyl group C ₁ -C _{4 alkyl} substituted by one or more hydroxyl groups or a -C (O) O ^-; R ' ₂ represents a C ₁ -C ₄ alkyl group optionally substituted by one or more hydroxyl groups; R ' ₃ and R' ₄ , which may be identical or different, represent a hydrogen atom, a hydroxyl group, a hydroxy (C ₁ -C ₄ ) alkyl group or -C (O) OR 'with R' representing an atom hydrogen, a C ₁ -C ₄ alkyl group or a -C (O) -O ^{- group} and in this case anionic counterion An ^- is absent, it being understood that only one of these two radicals R ' ₃ or R' ₄ can not represent a hydrogen atom; R ₃ represents a nitrogen atom or a group -C (O) OR "with R" representing a hydrogen atom, a C ₁ -C ₄ alkyl group or else R ₃ represents a group - C (O) -O ^- and in this case an anionic counterion An ^- is absent; N is 1 or 2; M is 0 or 1; T is 1 or 2; • An ^- represents anionic counterion; Y represents: i) a hydrogen atom; ii) an alkali metal; iii) an alkaline earth metal; iv) an ammonium group: N ⁺ R ^α R ^β R ^γ R ^δ , An ^- or a phosphonium group: P ⁺ R ^α R ^β R ^γ R ^δ , An ^- with R ^α , R ^β , R ^γ and R ^δ , identical or different, representing a hydrogen atom or a group (C ₁ -C ₄ ) alkylet An ^- is as defined above; or v) a thiol protecting group; Being heard that : the bond between the pyridinium ring and the double bond of the styryl group is positioned at the 2- or 4-position of the pyridinium; when n = 1, m = 1 then Y = H or protecting group of the thiol function and when n = 2, then m = 0. Fluorescent dye according to any one of claims 1, 6 and 7 of the following formula:

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36 with An ^- representing an anionic counterion. Dye composition comprising, in a suitable cosmetic medium, a fluorescent dye of formula (I) as defined in any one of Claims 1 to 8. Dyeing composition according to the preceding claim additionally containing at least one reducing agent. A process for dyeing keratinous materials, in which a suitable dyeing composition comprising at least one fluorescent dye of formula (I) as defined in any one of Claims 1 to 8, optionally in the presence of a reducing agent, is applied to the materials. . A process for dyeing keratin materials according to the preceding claim characterized in that the keratin materials are dark keratinous fibers having a pitch of less than or equal to 6. Multi-compartment device in which a first compartment contains a dye composition comprising a fluorescent dye of formula (I) as defined in claims 1 to 8 and a second compartment contains a reducing agent. Use of the fluorescent dyes of formula (I) as defined in claims 1 to 8 for dyeing particularly dark human keratin fibers particularly having a pitch of less than 6. Use according to the preceding claim for the lightening of dark keratin fibers particularly having a pitch of less than 6.